Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Urethral Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 18
- Active, not recruiting: 15
- Completed: 9
- Other: 8
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT02012699 — Integrated Cancer Repository for Cancer Research
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Nebraska |
| Enrollment | 999999 |
| Study Type | OBSERVATIONAL |
| Conditions | Pancreatic Cancer; Thyroid Cancer; Lung Cancer; Esophageal Cancer; Thymus Cancer |
The iCaRe2 is a multi-institutional resource created and maintained by the Fred & Pamela Buffett Cancer Center to collect and manage standardized, multi-dimensional, longitudinal data and biospecimens on consented adult cancer patients, high-risk individuals, and normal controls. The distinct characteristic of the iCaRe2 is its geographical coverage, with a significant percentage of small and …
NCT03866382 — Testing the Effectiveness of Two Immunotherapy Drugs (Nivolumab and Ipilimumab) With One Anti-cancer Targeted Drug (Cabozantinib) for Rare Genitourinary Tumors
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 314 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Adenocarcinoma; Bladder Clear Cell Adenocarcinoma; Bladder Mixed Adenocarcinoma; Bladder Neuroendocrine Carcinoma; Bladder Small Cell Neuroendocrine Carcinoma |
| Interventions | ; ; |
This phase II trial studies how well cabozantinib works in combination with nivolumab and ipilimumab in treating patients with rare genitourinary (GU) tumors that has spread from where it first started (primary site) to other places in the body. Cabozantinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such …
NCT04035642 — Single-Dose Image-Guided Radiotherapy With Urethral Sparing and DIL Boost for Intermediate-Risk Prostate Cancer (PROSINT II)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fundacao Champalimaud |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer |
| Interventions | ; ; |
This prospective single-arm phase II study evaluates the safety, feasibility, quality-of-life effects, PSA kinetics, imaging response, and clinical outcomes of definitive ultra-high dose single-fraction external beam radiation therapy in patients with biopsy-proven NCCN intermediate-risk localized adenocarcinoma of the prostate.
All eligible patients receive image-guided volumetric modulated a…
NCT04526353 — Early Oxybutinin Treatment for Boys With Posterior Urethral Valves
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Male Urogenital Diseases |
| Interventions |
Boys with posterior urethral valves have bladder dysfunction of varying severity. Early treatment of these children with anticholinergics is recommended by some teams, although there have never been any clear studies on the subject. To our knowledge, no comparative study of the evolution of valve bladders with or without treatment has been carried out to date.
Anticholinergic treatment, althou…
NCT04626167 — Concomitant Renal and Urinary Bladder Allograft Transplantation
| Status | Recruiting |
| Phase | Early Phase 1 |
| Sponsor | Mayo Clinic |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Kidney Diseases; Bladder Dysfunction; Bladder Absence; Posterior Urethral Valve; Neurogenic Bladder |
| Interventions |
The purpose of this study is to establish if concomitant renal and vascularized urinary bladder allograft transplantation is feasible.
NCT05383274 — Optilume PoST AppRoval Clinical Evaluation of Andrology ParaMeters
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Urotronic Inc. |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Stricture |
| Interventions |
Single-arm, prospective study assessing semen quality after treatment with the Optilume Urethral DCB in men between 22 and 65 years of age.
NCT05300685 — Peri-operative Oral Pain Control Following Buccal Graft Urethroplasty
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | University of California, San Francisco |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Stricture, Male |
| Interventions | ; ; |
Patients undergoing buccal urethroplasty will often have significant post-operative oral pain from the graft site. Various graft harvest techniques and methods for post-harvest hemostasis including graft site closure have been explored. Despite the frequency of this clinical scenario there is no established best practice for peri-operative pain management in this patient population. In addition…
NCT05804318 — Daily Adaptive Radiation Therapy Using an Individualized Approach for Prostate Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Varian, a Siemens Healthineers Company |
| Enrollment | 132 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer |
| Interventions |
This trial is a prospective, single-arm, multi-center clinical trial designed to assess whether adaptive radiotherapy with urethral sparing for low to intermediate risk localized prostate cancer will translate into a decreased rate of patient reported acute urinary side effects, as measured by the patient reported EPIC-26 questionnaire, compared with the historically reported rate for non-adapt…
NCT05969860 — At-Home Cancer Directed Therapy Versus in Clinic for the Treatment of Patients With Advanced Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Mayo Clinic |
| Enrollment | 220 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Anal Carcinoma; Advanced Biliary Tract Carcinoma; Advanced Bladder Carcinoma; Advanced Breast Carcinoma; Advanced Carcinoid Tumor |
| Interventions | ; ; |
This clinical trial studies the effect of cancer directed therapy given at-home versus in the clinic for patients with cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Currently most drug-related cancer care is conducted in infusion centers or specialty hospitals, where patients spend many hours a day isolated from f…
NCT07678489 — Total en Bloc Urethra Preservation at Robot-assisted Prostatectomy IDEAL Stage 2a
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Sami-Ramzi Leyh-Bannurah |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer (Localized), Urinary Incontinence (C61) |
| Interventions |
Prospective single-arm IDEAL stage 2a feasibility study of urethra-preserving RARP in localized prostate cancer.
NCT06369922 — TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Rochester |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Incontinence Female; Urinary Incontinence; Urinary Incontinence,Stress; Pain; Pain Acute |
| Interventions | ; |
This will be a double-blind randomized control trial in women with stress urinary incontinence who are undergoing an outpatient transurethral bulking procedure for stress urinary incontinence. Subjects will be identified by the University of Rochester urologists and urogynecologists participating in the study who currently oversee stress incontinence care. Subjects will be randomized into two g…
NCT06638931 — Agnostic Therapy in Rare Solid Tumors
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Instituto do Cancer do Estado de São Paulo |
| Enrollment | 28 |
| Study Type | INTERVENTIONAL |
| Conditions | Urachal Cancer; Parathyroid Carcinoma; Fibrolamellar Carcinoma; Angiosarcoma; Secretory Carcinoma of Breast |
| Interventions |
The ANTARES study is a phase II basket trial designed to evaluate the tissue-agnostic efficacy of the monoclonal anti-PD1 antibody, nivolumab, in patients with advanced or metastatic rare tumors.
The study aims to treat rare malignancies with PD-L1 expression (CPS ≥ 10), regardless of the tumor’s tissue type or location. Patients who have not responded to standard treatments will be included, …
NCT06754046 — BELIEVE Trial: Bulking vErsus sLing for Treating Stress Urinary IncontinEnce at the Time of Vaginal prolapsE Repair (BELIEVE)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospitals Cleveland Medical Center |
| Enrollment | 476 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Urinary Incontinence; Vaginal Prolapse |
| Interventions | ; |
The goal of this clinical trial is to learn if retropubic midurethral sling (RP-MUS) or bulkamide injection (PAHG) at the time of pelvic organ prolapse repair is better from the patient’s perspective. The main questions it aims to answer are:
What is the average difference in the urogenital distress inventory (UDI) long form score 24 months after surgery for each procedure? Which procedure has…
NCT07124000 — DESTINY-PANTUMOUR04
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Adenocarcinoma (NOS); Anal Cancer; Bladder Cancer; Cervical Cancer; Endometrial Cancer |
| Interventions |
This study will evaluate the effectiveness of T-DXd in patients with HER2-positive (IHC 3+) locally advanced, unresectable, or metastatic solid tumors who have received prior systemic treatment for metastatic or advanced disease and have no satisfactory alternative treatment options in a real-world setting in the US
NCT07627178 — A Prospective Comparative Study Evaluating the Safety and Efficacy of Transurethral Thulium Fiber Laser, Holmium Laser and Bipolar Enucleation of Large Sized Prostate
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Tanta University |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Benign Prostatic Hyperplasia (BPH); Lower Urinary Tract Symptom; Bladder Outlet Obstruction |
| Interventions | ; ; |
This study compares the safety and efficacy of three endoscopic enucleation techniques for large prostates (>100 mL) in patients with benign prostatic hyperplasia (BPH): Thulium Fiber Laser Enucleation (ThuFLEP), Holmium Laser Enucleation (HoLEP), and Bipolar Enucleation (B-TUEP). Ninety male patients with severe lower urinary tract symptoms (IPSS ≥20, Qmax ≤10 mL/s) who failed medical therapy…
NCT07217171 — A Study Evaluating the Safety, Efficacy, and Pharmacokinetics (PK) of EVOLVE104 in Participants With Advanced Urothelial and Squamous Cell Carcinomas
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | EvolveImmune United, Inc |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Cancer; Squamous Cell Carcinoma of the Lung; Esophageal Squamous Cell Carcinoma; Tongue Squamous Cell Carcinoma; Cutaneous Squamous Cell Cancer |
| Interventions | ; |
The goal of this study is to evaluate the safety and effectiveness of EVOLVE104 in participants with advanced urothelial and squamous cell carcinomas who have previously taken standard treatment options, have declined or have been ineligible for treatment with these medications. Participants with advanced or metastatic cancer who meet all eligibility criteria may be eligible to participate in t…
NCT07603011 — Effect of Catheter Duration on Prostate Laser Enucleation Surgery Outcomes in Patients With Urinary Retention
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Eskişehir Osmangazi University Medicine Faculty Hospital |
| Enrollment | 54 |
| Study Type | OBSERVATIONAL |
| Conditions | Urinary Retention; Benign Prostate Obstruction (BPO) |
| Interventions |
Benign Prostatic Obstruction (BPO) is a common condition in aging men that can lead to urinary retention, often requiring the use of an indwelling urinary catheter. While laser enucleation of the prostate (such as HoLEP, ThuLEP or ThuFLEP) is a safe and effective surgical treatment, it is not well understood how the length of time a patient spent with a urethral catheter before surgery affects …
NCT03258658 — Safety and Feasibility Study of Autologous Engineered Urethral Constructs for the Treatment of Strictures
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Urologic Diseases; Male Urogenital Diseases; Urethral Stricture; Urethral Injury |
| Interventions |
This is a Phase I clinical study to determine the safety and efficacy of using autologous, engineered urethral constructs for the treatment of urethral strictures in adult males.
The proposed study design is a prospective non-randomized and uncontrolled single-center investigation. Autologous urothelial cells (UCs) and smooth muscle cells (SMCs), obtained from enrolled male subjects’ bladder t…
Active, Not Recruiting
NCT00479128 — Bortezomib With Gemcitabine/Doxorubicin in Patients With Urothelial Cancer and Other Solid Tumors
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | M.D. Anderson Cancer Center |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Solid Tumor; Urethral Cancer |
| Interventions | ; ; |
The goal of this clinical research study is to find the highest tolerable dose of Gemzar® (gemcitabine) and Adriamycin® (doxorubicin) that can be given together with Velcade® (bortezomib) in patients with urothelial cancer or other solid tumors.
NCT02496208 — Cabozantinib S-malate and Nivolumab With or Without Ipilimumab in Treating Patients With Metastatic Genitourinary Tumors
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 152 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Small Cell Neuroendocrine Carcinoma; Bladder Squamous Cell Carcinoma; Bladder Urothelial Carcinoma; Clear Cell Renal Cell Carcinoma; Invasive Bladder Plasmacytoid Urothelial Carcinoma |
| Interventions | ; ; |
This phase I trial studies the side effects and best doses of cabozantinib s-malate and nivolumab with or without ipilimumab in treating patients with genitourinary (genital and urinary organ) tumors that have spread from where it first started (primary site) to other places in the body (metastatic). Cabozantinib s-malate may stop the growth of tumor cells by blocking some of the enzymes needed…
NCT02834013 — Nivolumab and Ipilimumab in Treating Patients With Rare Tumors
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 798 |
| Study Type | INTERVENTIONAL |
| Conditions | Acinar Cell Carcinoma; Adenoid Cystic Carcinoma; Adrenal Cortical Carcinoma; Adrenal Gland Pheochromocytoma; Anal Canal Neuroendocrine Carcinoma |
| Interventions | ; ; |
This phase II trial studies nivolumab and ipilimumab in treating patients with rare tumors. Immunotherapy with monoclonal antibodies, such as nivolumab and ipilimumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.
This trial enrolls participants for the following cohorts based on condition:
- Epithelial tumors of na…
NCT03291028 — Analysis of Primary and Metastatic Tumors in Patients With Renal Cell Carcinoma and Urothelial Carcinoma
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Fox Chase Cancer Center |
| Enrollment | 15 |
| Study Type | OBSERVATIONAL |
| Conditions | Renal Cell Carcinoma; Urothelial Carcinoma; Bladder Cancer; Ureter Cancer; Urethral Cancer |
| Interventions |
This is a comparative study using resected/ biopsied tumors samples collected from renal cell carcinoma and urothelial carcinoma patients who underwent surgical removal of lesions, followed by immune checkpoint blockade (ICB) treatment targting programmed cell death 1 (PD1) but developed new lesions later were also removed and stored in the biosample repository (BSR). The histology and genomic …
NCT03499964 — ROBUST III- Re-Establishing Flow Via Drug Coated Balloon For The Treatment Of Urethral Stricture Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Urotronic Inc. |
| Enrollment | 127 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Stricture |
| Interventions | ; |
ROBUST III is a prospective, multi-center, randomized controlled adaptive sample size clinical trial to establish the safety and effectiveness for the Optilume Stricture Drug Coated Balloon (DCB).
NCT03237780 — Atezolizumab With or Without Eribulin Mesylate in Treating Patients With Recurrent Locally Advanced or Metastatic Urothelial Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Bladder Urothelial Carcinoma; Locally Advanced Renal Pelvis Urothelial Carcinoma; Locally Advanced Ureter Urothelial Carcinoma; Locally Advanced Urethral Urothelial Carcinoma; Metastatic Bladder Urothelial Carcinoma |
| Interventions | ; ; |
This phase II trial studies the side effects of atezolizumab with or without eribulin mesylate and how well they work in treating patients with urothelial cancer that has come back (recurrent), spread to nearby tissues or lymph nodes (locally advanced), or spread from where it first started (primary site) to other places in the body (metastatic). Immunotherapy with monoclonal antibodies, such a…
NCT03682068 — Study of Durvalumab Given With Chemotherapy, Durvalumab in Combination With Tremelimumab Given With Chemotherapy, or Chemotherapy in Patients With Unresectable Urothelial Cancer
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 1246 |
| Study Type | INTERVENTIONAL |
| Conditions | Unresectable Locally Advanced Urothelial Cancer; Metastatic Urothelial Cancer |
| Interventions | ; ; |
This is a randomized, open-label, controlled, multi-center, global Phase III study to determine the efficacy and safety of combining durvalumab ± tremelimumab with standard of care (SoC) chemotherapy (cisplatin + gemcitabine or carboplatin + gemcitabine doublet) followed by durvalumab monotherapy versus SoC alone as first-line chemotherapy in patients with histologically or cytologically docume…
NCT04953104 — ARID1A and/or KDM6A Mutation and CXCL13 Expression
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | M.D. Anderson Cancer Center |
| Enrollment | 6 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Bladder Urothelial Carcinoma; Locally Advanced Renal Pelvis Urothelial Carcinoma; Locally Advanced Ureter Urothelial Carcinoma; Locally Advanced Urethral Urothelial Carcinoma; Locally Advanced Urothelial Carcinoma |
| Interventions | ; ; |
This phase II trial studies the effect of nivolumab in urothelial cancer that has spread to other places in the body (metastatic), specifically in patients with aberrations in ARID1A gene (ARID1A mutation) and correlate with expression level of CXCL13, an immune cytokine. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body’s immune system attack the cancer, and may in…
NCT05092958 — Testing the Addition of the Anti-cancer Drug, Cabozantinib, to the Usual Immunotherapy Treatment, Avelumab, in Patients With Metastatic Urothelial Cancer, MAIN-CAV Study
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 654 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Bladder Urothelial Carcinoma; Advanced Renal Pelvis Urothelial Carcinoma; Advanced Ureter Urothelial Carcinoma; Advanced Urethral Urothelial Carcinoma; Metastatic Bladder Urothelial Carcinoma |
| Interventions | ; ; |
This phase III trial compares the effect of adding cabozantinib to avelumab versus avelumab alone in treating patients with urothelial cancer that has spread from where it first started (primary site) to other places in the body (metastatic). Cabozantinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as …
NCT05186740 — ProVee Urethral Expander System IDE Study (ProVIDE)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | ProVerum Medical |
| Enrollment | 221 |
| Study Type | INTERVENTIONAL |
| Conditions | BPH With Symptomatic Lower Urinary Tract Symptoms |
| Interventions | ; |
A study to evaluate the safety, performance, and effectiveness of the ProVee Urethral Expander System (Investigational Device) when used in subjects with symptomatic urinary obstruction related to benign prostatic hyperplasia (BPH).
NCT04963153 — Testing Combination Erdafitinib and Enfortumab Vedotin in Metastatic Bladder Cancer After Treatment With Chemotherapy and Immunotherapy
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Bladder Urothelial Carcinoma; Locally Advanced Renal Pelvis Urothelial Carcinoma; Locally Advanced Ureter Urothelial Carcinoma; Locally Advanced Urethral Urothelial Carcinoma; Locally Advanced Urothelial Carcinoma |
| Interventions | ; ; |
This phase Ib trial evaluates the best dose, potential benefits, and/or side effects of erdafitinib in combination with enfortumab vedotin in treating patients with bladder cancer that has spread from where it first started (primary site) to other places in the body (metastatic) and possesses genetic alterations in FGFR2/3 genes. Erdafitinib is in a class of medications called kinase inhibitors…
NCT07484321 — Long-term Outcomes of Urethral Ligament Plication and Transvaginal Tape Surgery
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Sanliurfa Education and Research Hospital |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Urinary Incontinence (SUI) |
| Interventions | ; |
In the treatment of urinary incontinence caused by coughing, sneezing, or heavy lifting, the investigators will perform urinary tract tightening surgery, both with and without a sling, to address the relaxed urinary tract. The investigators would like to evaluate the one-year success and results of the sling or non-sling urinary tract tightening surgery the investigators will perform on the par…
NCT07384117 — Long-term Outcomes of Urethral and Uterosacral Ligament Plication
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Alev Esercan |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Incontinence Stress; Incontinence, Urge |
| Interventions |
The aim of this study is to determine the long-term success and outcomes of urethral ligament plication surgeries in patients with stress incontinence and uterosacral ligament plication surgeries in patients with urge incontinence.
NCT07554989 — Comparison of Concurrent Endoscopic Prostate Surgery With Botox-A Injection and Postoperative Medical Therapy in BPH Patients With Overactive Bladder Symptoms
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Taksim Egitim ve Arastirma Hastanesi |
| Enrollment | 70 |
| Study Type | OBSERVATIONAL |
| Conditions | Urinary Bladder, Overactive; Prostatic Hyperplasia, Benign; Bladder Outlet Obstruction; Botulinium Toxin-A |
Intravesical OnabotulinumtoxinA (BoNT-A) injection performed concurrently with endoscopic prostate surgery provides superior clinical improvement at the 12th postoperative week compared to standard medical therapy in patients with urodynamically confirmed bladder outlet obstruction (BOO) and concomitant overactive bladder (OAB). This superiority is demonstrated through significant improvements …
NCT07681843 — Early (Postoperative Day 3) Versus Standard (Postoperative Day 6) Urethral Catheter Removal After Living Donor Kidney Transplantation: A Prospective Randomized Controlled Trial
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Fahim Kanani |
| Enrollment | 172 |
| Study Type | INTERVENTIONAL |
| Conditions | Catheter-Associated Urinary Tract Infections (CAUTIs); Kidney Transplantation |
| Interventions | ; |
Urinary tract infection is one of the most common complications after kidney transplantation and is associated with increased morbidity, prolonged hospitalization, and impaired graft outcomes. The duration of urethral catheterization is a modifiable risk factor for catheter-associated urinary tract infection. This randomized controlled trial compares early catheter removal on postoperative day …
Not Yet Recruiting
NCT07550426 — The Effect of Periurethral Injection of Platelet Rich Plasma Versus Mid-urethral Sling in Treatment of Stress Urinary Incontinence : a Randomized Clinical Trial
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ain Shams University |
| Enrollment | 42 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Urinary Incontinence (SUI) |
| Interventions | ; |
this study used to compare efficacy between platelet rich plasma periurethral injection versus mid urethral sling ( trans obturator tape ) in treatment of stress urinary incontinence
NCT07555964 — Comparing Clean Intermittent Self-catheterization and Indwelling Catheterization for the Management of Urinary Retention Before BPH Surgery.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 106 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostatic Hyperplasia; Urinary Retention; Urinary Catheterization; Intermittent Urethral Catheterization; Urinary Tract Infections |
| Interventions | ; |
The CATHETERS trial is a multicenter, randomized, open-label superiority study comparing two methods of managing urinary retention before surgery for benign prostatic hyperplasia (BPH): clean intermittent self-catheterization (ICSC) versus indwelling catheter (IDC). The primary objective is to determine whether ICSC reduces the occurrence of infectious complications (urinary bacterial colonizat…
NCT07614854 — Effect of Prostatic Urethra and Seminal Vesicle Morphometry on Ejaculation
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Başakşehir Çam & Sakura City Hospital |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Premature Ejaculation; Ejaculation |
The goal of this observational study is to learn whether the size and shape of the prostatic urethra and seminal vesicles - measured on multiparametric prostate MRI (mpMRI) - are related to premature ejaculation (PE) severity in men aged 18-55.
The main questions it aims to answer are:
- Do men with premature ejaculation have different prostatic urethral length and angulation compared to men …
NCT07676942 — Intraoperative Lidocaine or Dexmedetomidine for Postoperative Pain Modulation After Urethral Reconstruction.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Centre of Postgraduate Medical Education |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Stricture |
| Interventions | ; ; |
The development of chronic postoperative pain (CPP) following surgery is influenced by several factors, among which the intensity of acute postoperative pain in the immediate perioperative period and mechanisms related to nerve fiber injury play a crucial role. Previous studies have demonstrated that factors such as the severity of early postoperative pain, patient age, and the extent of surgic…
NCT07668973 — Comparison Between Excision And Primary Anastomosis Urethroplasty And Tunica Vaginalis Graft Urethroplasty.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Sahiwal medical college sahiwal |
| Enrollment | 94 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Stricture; Erectile Dysfunction |
| Interventions | ; |
Urethroplasty is considered as a gold standard in treatment of urethral stricture disease having success rate of more than 93% in terms of recurrence of stricture. The objective of the study is to compare the outcome between excision and primary anastomosis (EPA) urethroplasty, a transecting urethroplasty technique and Tunica Vaginalis Graft (TVG) Urethroplasty, a non-transecting urethroplasty …
NCT07569874 — Thulium Laser Enucleation With Bladder Neck Incision for Small-Volume Benign Prostatic Hyperplasia
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Chinese PLA General Hospital |
| Enrollment | 615 |
| Study Type | INTERVENTIONAL |
| Conditions | Benign Prostatic Hyperplasia; Bladder Outlet Obstruction; Lower Urinary Tract Symptoms (LUTS) |
| Interventions | ; ; |
This study will evaluate the safety and effectiveness of thulium laser enucleation of the prostate combined with bladder neck incision in men with small-volume benign prostatic hyperplasia (BPH). Small-volume BPH may still cause significant bladder outlet obstruction and bothersome lower urinary tract symptoms, and the optimal surgical treatment for these patients remains uncertain.
In this mu…
Enrolling by Invitation
NCT07185698 — Urethral Vascularization and Urodynamics
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Insel Gruppe AG, University Hospital Bern |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Urinary Incontinence; Ultrasound; Vascularisation; Urodynamic Exam |
| Interventions |
The urethra plays a crucial role in maintaining urinary continence. Its complex blood supply is still not well understood. Particularly in the context of urethral pressure. Urethral pressure can be measured by bladder and urethral pressure studies (urodynamic).
This study aims to use advanced imaging techniques to analyse the blood supply of the urethra and correlate it to urethral pressure me…
Completed Trials
NCT00942331 — Gemcitabine Hydrochloride and Cisplatin With or Without Bevacizumab in Treating Patients With Advanced Urinary Tract Cancer
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 506 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Urothelial Carcinoma; Metastatic Bladder Urothelial Carcinoma; Metastatic Prostate Carcinoma; Metastatic Renal Pelvis Urothelial Carcinoma; Metastatic Ureter Urothelial Carcinoma |
| Interventions | ; ; |
This randomized phase III trial studies gemcitabine hydrochloride, cisplatin, and bevacizumab to see how well they work compared with gemcitabine hydrochloride and cisplatin in treating patients with urinary tract cancer that has spread to other places in the body. Drugs used in chemotherapy, such as gemcitabine hydrochloride and cisplatin, work in different ways to stop the growth of tumor cel…
NCT01352962 — Gemcitabine, Carboplatin, and Lenalidomide for Treatment of Advanced/Metastatic Urothelial Cancer and Other Solid Tumors
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Neoplasms; Neoplasms, Urethral; Cancer of the Urethra; Urethral Cancer |
| Interventions | ; ; |
Background:
- Gemcitabine and carboplatin are chemotherapy drugs used to treat several types of cancer, including cancer of the pancreas, bladder, ovaries, and lung. Lenalidomide, a drug that prevents the growth of new blood vessels in tumors, has been approved for treatment of certain blood cancers, but it has not yet been approved for use in combination with gemcitabine and carboplatin. Res…
NCT07592026 — Evaluation of Slit-like Adjusted Mathieu Versus Onlay Island Flap for Hypospadias Repair in Pediatrics
| Status | Completed |
| Phase | N/A |
| Sponsor | Al-Azhar University |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Narrow Urethral Plate Hypospadias |
| Interventions | ; |
- Purpose** To compare the Slit-like Adjusted Mathieu (SLAM) technique versus the inner transverse preputial onlay island flap for repair of anterior and mid-penile hypospadias with narrow urethral plate, evaluating complication rates, surgical outcomes, and cosmetic results.
- Methods** This prospective randomized controlled study included 80 patients with anterior and mid-penile hypospadi…
NCT05306145 — Comparison of H-FIRE and TURP in Treating Benign Prostatic Hyperplasia
| Status | Completed |
| Phase | N/A |
| Sponsor | Shanghai East Hospital |
| Enrollment | 118 |
| Study Type | INTERVENTIONAL |
| Conditions | Benign Prostatic Hyperplasia |
| Interventions | ; |
This trial is comparing the effects and safety in treating men with benign prostatic hyperplasia between high freqnence irreversible electroporation and trans urethral resection prostate.
NCT05463991 — Bioengineered Collagen Implant for Urethral Stricture Repair
| Status | Completed |
| Phase | N/A |
| Sponsor | Regenosca SA |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Stricture |
| Interventions |
The field of research for this study is tissue engineering and the utilization of a bioengineered collagen implant as a substitute biomaterial for conventional buccal mucosa in substitution urethroplasty of distal urethral strictures.
NCT07460167 — Penile Rehabilitation in Patients With Erectile Dysfunction After Pelvic Fracture Urethral Injury Using Low-intensity Shock Wave.
| Status | Completed |
| Phase | N/A |
| Sponsor | South Valley University |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions |
the efficacy and safety of low intensity shock wave therapy (LiSWT) as an ED treatment. Olsen et al. demonstrated that LiSWT might be a possible solution in some ED patients of organic origin . The clinical results revealed that LiSWT was beneficial to ED patients nonresponsive to phosphodiesterase type 5 inhibitors (PDE5i) Animal studies revealed that LiSWT significantly improved ischemic musc…
NCT07587333 — Convective Radio-frequency Water Vapor Energy Verses Trans-urethral Enucleation of Prostate for Management of Benign Prostatic Hyperplasia
| Status | Completed |
| Phase | N/A |
| Sponsor | Beni-Suef University |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | BPH (Benign Prostatic Hyperplasia) |
| Interventions | ; |
Convective RF water vapor energy was introduced as a minimally invasive, radio-frequency thermal energy-based treatment, designed to convectively deliver sterile water vapor, or steam for targeted ablation limited to the transition and central zones in men with clinical BPH. Thus. the aim of the study is to compare Convective RF water vapor energy (Rezum) with trans-urethral enucleation of the …
NCT07645456 — BOTOX Injection Technique for LUTS Due to BPH
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Benha University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Benign Prostatic Hyperplasia |
| Interventions |
his prospective, randomized comparative study evaluated whether a combined Botulinum Toxin Type A (BOTOX) injection technique provides superior outcomes compared to injecting the prostatic parenchyma alone for patients with benign prostatic hyperplasia (BPH) and a prostate volume of 30-60 grams. Sixty men with persistent, medically refractory lower urinary tract symptoms (LUTS) were divided equ…
NCT07505316 — Holmium Laser Versus Cold Knife Treatment in Urethral Strictures
| Status | Completed |
| Phase | N/A |
| Sponsor | Shahida Islam Medical Complex |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Stricture Urethra; Holmium Laser; Recurrence |
| Interventions | ; |
The goal of this study is to assess the efficacy of optical internal urethrotomy, which uses a holmium laser in comparison to a cold knife, in treating short-segment urethral strictures in our local setting. The study will help standardize treatment protocols for urethral stricture based on functional results. The local findings will encourage adoption of minimally invasive laser techniques in …
Other (Terminated)
NCT01095692 — Evaluating the Necessity of TOT Implantation in Women With Pelvic Organ Prolapse and Occult Stress Urinary Incontinence
| Status | Terminated |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 21 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Urinary Incontinence; Pelvic Organ Prolapse |
| Interventions | ; |
Nowadays the clinical significance of an occult stress urinary incontinence and its optimal treatment is not known.Regarding treatment, there are 2 main approaches : either the systematic preventive treatment of the occult stress urinary incontinence by means of a tension free vaginal tape (TOT) together with the treatment of prolapse or the treatment of prolapse in the first place and treatmen…