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 Penis Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 18
- Active, not recruiting: 10
- Completed: 14
- 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 …
NCT04923178 — A Multi-Center Natural History of Urothelial Cancer and Rare Genitourinary Tract Malignancies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1100 |
| Study Type | OBSERVATIONAL |
| Conditions | Urothelial Cancer; Bladder Cancer; Genitourinary Cancer; Urogenital Neoplasms; Urogenital Cancer |
Background:
Tumors in the genitourinary tracts can occur in the kidney, bladder, prostate, and testicles and can have common and rare histologies. Some cancers that occur along the genitourinary (GU) tract are rare. Some GU tumors are so rare that they are not included in treatment studies or tissue banks. This makes it hard for researchers to determine standards of care. Researchers want to l…
NCT05686226 — E7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Christian Hinrichs |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Cancer; Throat Cancer; Oropharynx Cancer; Anal Cancer; Vulva Cancer |
| Interventions | ; |
This is a phase II clinical trial to assess the clinical activity of immunotherapy with E7 TCR-T cells for metastatic HPV-associated cancers. HPV-associated cancers in include cervical, throat, penile, vulvar, vaginal, anal, and other cancers. Participants will receive a conditioning regimen, E7 TCR-T cells, and aldesleukin. Clinical response to treatment will be determined.
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…
NCT06104618 — Enfortumab Vedotin for the Treatment of Patients With Metastatic or Unresectable Squamous Cell Carcinoma of the Penis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Mayo Clinic |
| Enrollment | 28 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Penile Squamous Cell Carcinoma; Stage III Penile Cancer AJCC v8; Stage IV Penile Cancer AJCC v8; Unresectable Penile Squamous Cell Carcinoma |
| Interventions | ; ; |
This phase II trial tests how well enfortumab vedotin works for treating patients with squamous cell carcinoma of the penis that has spread to other places in the body (metastatic) or cannot be removed by surgery (unresectable). Enfortumab vedotin is a monoclonal antibody, enfortumab, linked to an anticancer drug called vedotin. It works by helping the immune system to slow or stop the growth o…
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, …
NCT06832280 — Improving Parental Support in Hypospadias Care
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of North Carolina, Chapel Hill |
| Enrollment | 324 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias |
| Interventions | ; |
The proposed study will enroll parent-child pairs and is designed to obtain new knowledge and improve hypospadias care. Parent-child pairs will be randomized into different groups over 36 months and participate for at least 6 months.
NCT06966375 — Worldwide Yearly Screening for Hypospadias
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Wisconsin, Madison |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias |
| Interventions |
The purpose of this study is to recruit approximately 20 male participants who have a history of repaired hypospadias to test the feasibility and acceptability of the Care Planning Tool within the Worldwide Yearly Screening for Hypospadias (WYSH) Web Application.
NCT05639972 — E7 T-cell Receptor (TCR) -T Cell Induction Therapy for Locoregionally Advanced HPV-associated Cancers
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Christian Hinrichs |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | HPV-Associated Cervical Carcinoma; HPV-Related Carcinoma; HPV-Related Malignancy; HPV Positive Oropharyngeal Squamous Cell Carcinoma; HPV-Related Adenocarcinoma |
| Interventions | ; |
The goal of this study is to determine the feasibility of administration of a single dose of E7 TCR-T cells as induction therapy prior to definitive treatment (chemoradiation or surgery) of locoregionally advanced HPV-associated cancers. The intent of E7 TCR-T cell treatment is to shrink or eliminate tumors and thereby facilitate definitive therapy and increase overall survival.
This study see…
NCT06989593 — Breaking Silence Through Story: A Narrative Medicine Intervention for Parents of Children With Urogenital Conditions
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Sarah Schlegel |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | DSD; Hypospadias |
| Interventions |
The goal of this clinical trial is to learn whether a journaling intervention can reduce stress and anxiety in parents of children with urogenital conditions (such as differences of sex development and hypospadias).
The main questions it aims to answer are:
- Does guided journaling help to reduce anxiety levels in parents of children with urogenital conditions?
- What are parents’ perspective…
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…
NCT07675798 — Effect of Caudal Block on Urethrocutaneous Fistula After Distal Hypospadias Repair
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias; Caudal Block; Pediatric Anesthesia |
| Interventions | ; |
Hypospadias is one of the most common congenital urogenital anomalies in males, occurring in approximately 1 in every 200-300 male births. It is characterized by abnormal positioning of the urethral meatus on the ventral surface of the penis. Surgical repair is the standard treatment; however, urethrocutaneous fistula formation remains one of the most frequent and clinically significant postope…
NCT07619651 — Comparison of Sacral ESP Block and Caudal Block in Pediatric Hypospadias Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | TC Erciyes University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias; Postoperative Pain |
| Interventions | ; |
Hypospadias surgery in pediatric patients requires effective postoperative analgesia to ensure patient comfort and reduce perioperative stress. Caudal epidural block is widely used for analgesia in pediatric urological procedures; however, alternative regional techniques such as the sacral erector spinae plane (ESP) block have recently gained attention.
This prospective comparative study aims …
NCT07054307 — MRG003 Plus HX008 as First-Line Treatment for EGFR-Positive Locally Advanced or Metastatic Penile Squamous Cell Carcinoma
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Jiyan Liu |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Penile Cancer |
| Interventions | ; |
Penile squamous cell carcinoma (PSCC) is a rare malignancy, with stage IV patients exhibiting a 2-year overall survival (OS) rate of 21% and a 5-year survival rate of 0%. Both the National Comprehensive Cancer Network (NCCN) and European Association of Urology (EAU) guidelines recommend chemotherapy as the first-line treatment. However, the efficacy of chemotherapeutic agents in PSCC remains su…
NCT07426731 — Comparison of Sacral ESP Block and Dorsal Penile Nerve Block in Pediatric Hypospadias Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Medipol University |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Postoperative Pain; Hypospadias |
| Interventions | ; |
This randomized controlled trial aims to compare the postoperative analgesic efficacy of ultrasound-guided Sacral Erector Spinae Plane (ESP) block versus Dorsal Penile Nerve Block (DPNB) in pediatric patients aged 1-7 years undergoing hypospadias surgery. The primary outcome is the pain score assessed by the FLACC scale at the 12th postoperative hour
NCT07384416 — QL1706 Plus Lenvatinib in Previously Treated Penile Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Sun Yat-sen University |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Penile Cancer |
| Interventions |
This phase II clinical study aims to evaluate the efficacy and safety of QL1706 in combination with lenvatinib in patients with previously treated advanced or metastatic penile squamous cell carcinoma.
The primary objective of the study is to determine the median progression-free survival (PFS) of this regimen according to RECIST 1.1 criteria. Secondary objectives include evaluating objective …
NCT07378670 — DEfeating PEnile CAncer-2
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital Tuebingen |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Penile Cancer; Penile Neoplasms Malignant |
| Interventions | ; |
Open inguinal lymphadenectomy (O-ILAD) is the current standard of care for invasive staging and simultaneously the curative approach for patients with PeCa and elevated risk for or clinically detectable lymphatic disease in the groin. The high rate of complications of this surgical procedure, which are often mutilating and associated with a long-term convalescence, leads to a critical delay in …
Active, Not Recruiting
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…
NCT03391479 — A Study of Avelumab in Penile Cancer Who Are Unfit for or Have Progressed After Platinum-Based Chemotherapy
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | University Health Network, Toronto |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Penile Cancer; Advanced Cancer; Metastatic Cancer |
| Interventions | ; |
This is a phase 2 study whose purpose is see how useful investigational drug, avelumab, is in patients with locally advanced or metastatic penile cancer who are unfit for or progressed on platinum-based chemotherapy.
The usefulness of avelumab in this study population will be determined by anti-tumor activity assessed by objective response rate.
Avelumab is a monoclonal antibody that binds to…
NCT04432597 — HPV Vaccine PRGN-2009 Alone or in Combination With Anti-PDL1/TGF-Beta Trap (M7824) in Subjects With HPV Associated Cancers
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 39 |
| Study Type | INTERVENTIONAL |
| Conditions | HPV Positive Cancer; Vulvar, Vaginal, Penile, Rectal Cancer; Anal Cancer; Oropharyngeal Cancer; Cervical Cancer |
| Interventions | ; ; |
Background:
For some cancers associated with human papillomavirus (HPV), standard treatments are not helpful. Researchers want to see if a vaccine for HPV combined with a drug called M7824 (MSB0011359C) has a better effect on these cancers than when they work alone.
Objective:
To find a safe dose of HPV vaccine alone or combined with M7824. Also, to test if either HPV vaccine alone or combin…
NCT04491942 — Testing the Addition of an Anti-cancer Drug, BAY 1895344, to the Usual Chemotherapy Treatment (Cisplatin, or Cisplatin and Gemcitabine) for Advanced Solid Tumors With Emphasis on Urothelial Cancer
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 74 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Bile Duct Carcinoma; Advanced Breast Carcinoma; Advanced Cervical Carcinoma; Advanced Endometrial Carcinoma; Advanced Esophageal Carcinoma |
| Interventions | ; ; |
This phase I trial identifies the best dose, possible benefits and/or side effects of BAY 1895344 in combination with chemotherapy in treating patients with solid tumors or urothelial cancer that has spread to other places in the body (advanced). BAY 1895344 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Cisplatin and gemcitabine are chemotherapy drug…
NCT04708470 — A Phase I/II Study of Combination Immunotherapy for Advanced Cancers Including HPV-Associated Malignancies, Small Bowel, and Colon Cancers
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 55 |
| Study Type | INTERVENTIONAL |
| Conditions | Oropharyngeal Cancer; Neck Cancer; Human Papillomavirus; HPV; Anal Cancer |
| Interventions | ; ; |
Background:
Often, metastatic human papillomavirus (HPV) associated cancers cannot be cured. They also do not respond well to treatment. Some forms of colon cancer also have poor responses to treatment. Researchers want to see if a new drug treatment can help people with these types of cancers.
Objective:
To find a safe dose of entinostat in combination with PDS01ADC and bintrafusp alfa and …
NCT03849586 — Registry for Patients Undergoing Penile Prosthesis Implantation for Male Erectile Dysfunction
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | European Association of Urology Research Foundation |
| Enrollment | 1076 |
| Study Type | OBSERVATIONAL |
| Conditions | Erectile Dysfunction |
Prospective collection of pre-defined parameters on the surgical treatment of male erectile dysfunction using Penile Prosthesis Implants (PPIs).
NCT05946993 — Linking In With Advice and Supports for Men Impacted by Metastatic Cancer
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University College Cork |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Survivorship; Prostate Cancer; Kidney Cancer; Urothelial Tract/Bladder Cancer, Nos; Testicular Cancer |
| Interventions | ; ; |
To evaluate the feasibility of introducing a men’s cancer survivorship programme into routine follow up care in patients with advanced genitourinary malignancies.
NCT05777031 — Safety and Efficacy of Collagenase Clostridium Histolyticum After Prior Intralesional PRP for Peyronie’s Disease
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | University of Miami |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Peyronie Disease; Sexual Dysfunctions, Psychological; Genital Diseases, Male |
| Interventions |
The purpose of this study is to learn about the safety and side effects of intralesional collagenase clostridium histolyticum (CCH) injected into the Peyronies Disease (PD) plaque after receiving prior treatment with intralesional Platelet Rich Plasma (PRP) injections.
NCT07118176 — Determining the Biodistribution of an Imaging Tracer (68Ga-FAPi-46) in Patients With Solid Tumors or Hematologic Cancers
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Jonsson Comprehensive Cancer Center |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Anal Carcinoma; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma; Cholangiocarcinoma |
| Interventions | ; ; |
This phase I trial is evaluating a new imaging tracer (68Ga-FAPi-46) with positron emission tomography (PET)/computed tomography (CT) to determine where and to which degree the tracer (68Ga-FAPi-46) accumulates in normal and cancer tissues (the biodistribution) in patients with solid tumors or hematologic (blood) cancers. PET is an established imaging technique that utilizes small amounts of ra…
Not Yet Recruiting
NCT07497919 — A Study of Becotatug Vedotin Combined With Pucotenlimab in the Treatment of EGFR-Positive Advanced Penile Cancer
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Fudan University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Penile Cancer |
| Interventions |
Penile cancer is a rare malignant tumor of the male genitourinary system, with 95% being squamous cell carcinoma. Due to social factors, delayed diagnosis is common, leading to a high rate of lymph node metastasis (17%-45% at diagnosis), which significantly impairs quality of life and prognosis. The 5-year survival rate is 27% for patients with lymph node metastasis and 0%-17% for those with pe…
NCT07685249 — Rehabilitation and Sex Therapy to Optimize Recovery After Prostate Cancer Treatment
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Urinary Incontinence; Erectile Dysfunction |
| Interventions | ; ; |
This study is being done at Duke Health and includes adult men who have been treated for localized prostate cancer. The goal is to see if it is feasible and acceptable to offer sex therapy by telehealth after prostate cancer treatment.
All participants receive pelvic floor physical therapy and education about penile rehabilitation, including use of a vacuum erection device. Participants are ra…
NCT07602894 — Analgesia for Perineal Surgeries in High-risk Pediatric Patients
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Zagazig University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Analgesia |
| Interventions | ; |
Perioperative pain management in pediatric patients, especially for anorectal and penile surgeries, presents significant challenges for anesthetists. Complications associated with systemic analgesia, such as respiratory issues, cardiovascular problems, and neurological effects, can be avoided by using regional anesthesia. This study aims to evaluate the effectiveness of Ultrasound-Guided Sacral…
NCT07518979 — EGFR-ADC (Becotatug Vedotin) Combined With PD-1 Inhibitor (Pucotenlimab) in Neoadjuvant Treatment of Advanced Penile Cancer
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Jiyan Liu |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Penile Cancer |
| Interventions | ; |
This clinical study is a Phase II research trial focused on a new preoperative treatment for men with advanced penile squamous cell carcinoma (a type of penile cancer). The cancer may be hard to treat with penile-sparing surgery, or it may have spread to nearby lymph nodes (like groin lymph nodes).
We are testing a combination of two medicines: Becotatug vedotin (a targeted therapy that finds …
NCT07240649 — Emerging Indications for Hyperbaric Oxygen Treatment
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Jay C. Buckey Jr. |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Post-COVID-19 Condition; Ulcerative Colitis; Crohn Disease; Calciphylaxis; Frostbite |
| Interventions | ; |
This study will evaluate the effectiveness of hyperbaric oxygen therapy (HBOT) on treating emerging indications (i.e., conditions that have shown to potentially benefit from HBOT) using the Multicenter Registry for Hyperbaric Oxygen Treatment. The study team aims to collect ongoing data on how well HBOT treats these emerging indications, and to add these data to the growing HBO Registry. The re…
NCT07246642 — IPP Placement & Intracavernosal Block
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction (ED) |
| Interventions |
The inflatable penile prosthesis (IPP) is the gold standard for surgical management of erectile dysfunction (ED) and there is no consensus on the best postoperative pain management regimen. In the wake of the opioid epidemic, postoperative pain management is heavily scrutinized. The National Institute of Health estimated over 81,000 individuals died following overdose of any opioids in 2022 alo…
NCT03463239 — Bioengineered Penile Tissue Constructs for Irreversibly Damaged Penile Corpora
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Urologic Diseases; Male Urogenital Diseases; Penile Diseases; Corpus Callosum Malformation; Corpora Cavernosa; Inflammation |
| Interventions |
The primary objective of this clinical trial is to evaluate the safety of autologous engineered corpora cavernosa + albuginea constructs for treatment of complex penile deformities. Autologous endothelial and smooth muscle cells obtained from enrolled subjects’ corpora cavernosa biopsy sample, will be culture expanded in vitro and used to seed decellularized corpora cavernosa + albuginea obtain…
Enrolling by Invitation
NCT06565663 — MaPGAS Decision Making
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Dartmouth-Hitchcock Medical Center |
| Enrollment | 140 |
| Study Type | INTERVENTIONAL |
| Conditions | Gender Dysphoria; Gender Dysphoria, Adult; Gender Incongruence; Transgenderism; Transsexualism |
| Interventions |
The goal of this clinical trial is to test a new online tool designed to provide clear and understandable information to help individuals considering Metoidioplasty and Phalloplasty Gender Affirming Surgery (MaPGAS)make informed decisions
The main questions it aims to answer are:
- How user-friendly is the decision aid for individuals considering metoidioplasty and phalloplasty?
- Does using …
Completed Trials
NCT00210041 — Phase 2 Study of Association Gemcitabine-Cisplatin to Treat Penis Epidermoid Carcinoma
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Institut Claudius Regaud |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Genital Neoplasms, Male |
| Interventions | ; |
The purpose of this study is to determine whether association Gemcitabine-Cisplatin is effective in the treatment of penis epidermoid carcinoma loco-regionally advanced or metastatic.
NCT00582231 — Penile Injection Anxiety
| Status | Completed |
| Phase | N/A |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 126 |
| Study Type | OBSERVATIONAL |
| Conditions | Penile Injection Therapy; Erectile Dysfunction; Radical Pelvic Surgery |
| Interventions |
The purpose of this study is to help us understand more about your experience with penile injection therapy. Many men become anxious when thinking about penile injections. We would like to understand more about this anxiety. You will be asked to fill out questionnaires before you start penile injection training, at each training visit, and then at your four month follow-up visit.
NCT02379520 — HPV-16/18 E6/E7-Specific T Lymphocytes, Relapsed HPV-Associated Cancers, HESTIA
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Baylor College of Medicine |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Human Papillomavirus-Related Carcinoma; Human Papillomavirus Positive Oropharyngeal Carcinoma; Human Papillomavirus Positive Cervical Carcinoma; Human Papillomavirus Positive Anal Carcinoma; Human Papillomavirus Positive Vulvar Carcinoma |
| Interventions | ; ; |
Subjects have a type of cancer that has been associated with an infection with a virus called human papilloma virus (HPV). The cancer has come back, has not gone away after standard treatment or the subject cannot receive standard treatment.
This is a research study using special immune system cells called HPVST cells, a new experimental treatment.
Investigators want to find out if they can u…
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…
NCT04287868 — Combination Immunotherapy in Subjects With Advanced HPV Associated Malignancies
| Status | Completed |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 51 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Cancer; HPV Cancers; Anal Cancer; Oropharyngeal Cancer; Vulvar, Vaginal, Penile, Rectal Cancer |
| Interventions | ; ; |
Background:
More than 30,000 cases of human papillomavirus (HPV) associated cancers occur annually in the United States. When these cancers spread, they do not respond well to standard treatments and are often incurable. Researchers want to see if a mix of drugs can help.
Objective:
To learn if a mix of immunotherapy drugs can shrink tumors in people with HPV associated cancers.
Eligibility…
NCT04718584 — the Efficacy and Safety of LDP in Patients With Urinary and Male Genital Tumors
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Dragonboat Biopharmaceutical Company Limited |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Cancer; Renal Carcinoma; Advanced Penile Carcinoma |
| Interventions |
This is a single-arm,open, multicenter, phase II clinical study of the efficacy and safety of human anti-PD-L1 monoclonal antibody Injection (LDP) in the treatment of urinary and male genital tumors.
NCT07495176 — USC-Exos in Corpus Spongiosum Reconstruction for Hypospadias
| Status | Completed |
| Phase | N/A |
| Sponsor | Shanghai Children’s Hospital |
| Enrollment | 82 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias |
| Interventions | ; |
Hypospadias is one of the common congenital malformation disorders in male children, with a ratio of about 1 to 300 in newborn boys. Proximal hypospadias, due to the underdeveloped corpus spongiosum, has a high incidence of postoperative complications (e.g., urethral fistula, stricture, recurrence of penile curvature), exceeding 50%. Traditional surgeries focus on urethral tubularization but fa…
NCT05461430 — Mass Response of Tumor Cells as a Biomarker for Rapid Therapy Guidance (TraveraRTGx)
| Status | Completed |
| Phase | N/A |
| Sponsor | Travera Inc |
| Enrollment | 72 |
| Study Type | OBSERVATIONAL |
| Conditions | Pleural Effusion, Malignant; Ascites, Malignant; Carcinoma; Carcinoma, Hepatocellular; Carcinoma, Renal Cell |
The primary objective of this study, sponsored by Travera Inc. in Massachusetts, is to validate whether the mass response biomarker has potential to predict response of patients to specific therapies or therapeutic combinations using isolated tumor cells from various specimen formats including malignant fluids such as pleural effusions and ascites, core needle biopsies, fine needle aspirates, o…
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…
NCT07615335 — Comparison Between Ultrasound Guided Caudal Block and Ultrasound Guided Dorsal Penile Block in Hypospadias Surgery in Children
| Status | Completed |
| Phase | N/A |
| Sponsor | Ahmed Aouf |
| Enrollment | 62 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias; Hypospadias, Coronal |
| Interventions | ; |
The study focuses on comparing the caudal block (CB) and the dorsal penile nerve block (DPNB) via ultrasound guidance in regional anesthesia in hypospadias surgery.
NCT07525570 — Effect of Adding Byar’s Flap to Double Dartos Coverage in TIP Urethroplasty for Distal Hypospadias: A Randomized Trial
| Status | Completed |
| Phase | N/A |
| Sponsor | Javaid Afridi |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias; Distal Penile Hypospadias (Disorder) |
| Interventions | ; |
This randomized controlled trial evaluates the effect of adding Byar’s flap in combination with double dartos flap coverage during tubularized incised plate (TIP) urethroplasty in children with distal hypospadias. The study compares surgical outcomes between two techniques: TIP urethroplasty with double dartos coverage alone versus TIP urethroplasty with double dartos plus Byar’s flap reinforce…
NCT06862271 — Comparison of Caudal Block Combined With General Anesthesia and Penile Block and Intravenous Fentanyl in Pediatric Surgeries
| Status | Completed |
| Phase | N/A |
| Sponsor | Miray Gözde Özdemir |
| Enrollment | 120 |
| Study Type | OBSERVATIONAL |
| Conditions | Caudal Block; Pediatric Urologic Surgeries; Fentanyl; Pediatric Delirium; Analgesia |
| Interventions | ; |
Urogenital surgery is one of the most frequently performed surgical procedures in the pediatric patient population. There is no consensus on which analgesic method is most effective for pain control in these patients. In clinical practice, if there are no contraindications, caudal block or penile block combined with intravenous fentanyl can be preferred as an analgesic method.
In this study, t…
NCT07602608 — Platelet-Rich Plasma With or Without Tadalafil for Erectile Dysfunction
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Benha University |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; |
Platelet-rich plasma is being studied as a regenerative treatment option for erectile dysfunction, but it is unclear whether adding daily tadalafil gives additional benefit over platelet-rich plasma alone. This study evaluates adult men with mild to mild-moderate erectile dysfunction who had an inadequate response to previous phosphodiesterase type 5 inhibitor treatment.
Participants were rand…
NCT07575204 — Ultrasound-Guided Pudendal vs Dorsal Penile Nerve Block for Pediatric Hypospadias Surgery
| Status | Completed |
| Phase | N/A |
| Sponsor | Bangladesh Medical University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypospadias; Pudendal Nerve Block; Penile Nerve Block; Postoperative Pain |
| Interventions | ; |
The goal of this clinical trial is to compare the effectiveness and safety of two regional anesthesia techniques, ultrasound-guided pudendal nerve block and dorsal penile nerve block, for postoperative pain management in children undergoing hypospadias surgery.
The main questions we aim to answer are:
Which technique provides more effective pain relief after surgery? What are the potential si…