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 Erectile Dysfunction from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 18
- Active, not recruiting: 8
- Completed: 11
- Other: 13
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00499317 — Genetic Study of Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Boston Children’s Hospital |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Prostatitis (CP); Chronic Pelvic Pain Syndrome (CPPS); Painful Bladder Syndrome (PBS); Benign Frequency Syndrome (BFS); Interstitial Cystitis |
Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) is a condition with several causes of which some remain unknown. It is believed that some types of CP may be genetic or passed down (inherited) from one generation to the next.
In this study, we are collecting genetic material and medical information to try to determine if genetic factors play a role in CP/CPPS. We will be collecting D…
NCT02706561 — Helping Men Adhere to Sexual Rehabilitation Following Prostate Cancer Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 224 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Erectile Dysfunction |
| Interventions | ; ; |
The purpose of this study is to test two different ways to help men with sexual rehabilitation.
NCT04861194 — EREctile Function Preservation for Prostate Cancer Radiation Therapy (ERECT)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | UMC Utrecht |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Erectile Dysfunction Following Radiation Therapy |
| Interventions |
Single-arm phase II trial of 70 men with low- or intermediate-risk prostate cancer receiving magnetic resonance guided adaptive radiotherapy (MRgRT) in 5 fractions of 7.25 Gy, additionally sparing the neurovascular bundles, the internal pudendal arteries, the corpora cavernosa, and the penile bulb for erectile function preservation.
NCT05650866 — Safety and Tolerability of a Novel Implantable Device for the Treatment of Erectile Dysfunction
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Comphya Australia |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction Following Radical Prostatectomy |
| Interventions |
The goal of this clinical trial is to assess if a new device is safe to use as a potential treatment for erectile dysfunction following radical prostatectomy.
The main questions it aims to answer are:
- Is the device safe?
- Does the device works well? Are the participants satisfied with the device?
Participants will be implanted with the device during the ongoing prostatectomy surgery and w…
NCT05109208 — The Use of Ultrasound in Assessing Post-prostatectomy Erectile Dysfunction
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Mayo Clinic |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Adenocarcinoma |
| Interventions |
Researchers are trying to determine whether there is additional utility to using vibroelastography, a noninvasive ultrasound technique to evaluate for the presence of tissue fibrosis, in conjunction with standard penile duplex Doppler ultrasound to assess erectile function (recovery) after prostate cancer surgery.
NCT06167733 — Safety and Efficacy of the VERTICA® RF Device for the Treatment of ED
| Status | Recruiting |
| Phase | N/A |
| Sponsor | OHH-MED Medical Ltd |
| Enrollment | 98 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; |
Adult subjects with mild to moderate and moderate ED who meet the study eligibility criteria will be enrolled in the study. The enrolled subjects will be randomized by a 1:1 ratio to receive the Active or Sham VERTICA® treatment. Baseline assessments will include collection of demographic data, medical history, concomitant medications and baseline clinical examinations. The initial treatment se…
NCT07592533 — A Single Arm Study of Extracorporeal Shockwave Therapy for Management of Erectile Dysfunction
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of California, San Francisco |
| Enrollment | 157 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions |
This is a device study (while the device has been patented and cleared by the FDA, the indication of the use for Erectile Dysfunction has been yet approve). EXSTACY is a study to collect information on which patients who have trouble getting or keeping an erection rigid enough for sex (sometimes known as Erectile Dysfunction or ED) benefit from light intensity shockwave therapy (LI-SWT). LI-SWT…
NCT07431008 — Safety Follow-up Study of Cellgram-ED in Post-Radical Prostatectomy Erectile Dysfunction
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Pharmicell Co., Ltd. |
| Enrollment | 32 |
| Study Type | OBSERVATIONAL |
| Conditions | Erectile Dysfunction |
This phase II clinical trial with safety follow-up is designed to evaluate the efficacy and safety of Cellgram-ED (autologous bone marrow-derived mesenchymal stem cells) administered via intracavernous injection in patients with erectile dysfunction after radical prostatectomy.
NCT07480161 — Mesenchymal Stem Cell and Exosome Therapy for Diabetic Erectile Dysfunction
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Ankara City Hospital Bilkent |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction With Diabetes Mellitus |
| Interventions | ; ; |
The goal of this prospective randomized controlled clinical study is to evaluate the effectiveness and safety of intracavernosal injections of umbilical cord-derived mesenchymal stem cells (MSCs) and umbilical cord-derived MSC-derived exosomes in men aged 25 to 75 years with diabetic erectile dysfunction (ED) who have not responded adequately to conventional medical treatments such as phosphodi…
NCT07487181 — A Survey of Traditional Medicine Pattern Identification in Patients With Erectile Dysfunction
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Medicine and Pharmacy at Ho Chi Minh City |
| Enrollment | 375 |
| Study Type | OBSERVATIONAL |
| Conditions | Erectile Dysfunctions |
Erectile dysfunction (ED) is a common condition that significantly affects quality of life, psychological well-being, and interpersonal relationships. In Traditional Medicine, ED is classified into different syndrome patterns, which are essential for guiding individualized treatment; however, evidence on their distribution and associated factors in Vietnam remains limited. This cross-sectional …
NCT07597798 — EVERiST: Impact of Image Detected Accessory Pudendal Artery on Erection Recovery After Nerve Sparing Prostatectomy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University College, London |
| Enrollment | 40 |
| Study Type | OBSERVATIONAL |
| Conditions | Radical Prostatectomy; Erectile Dysfunction Following Radical Prostatectomy; Erectile Dysfunction Due to Arterial Insufficiency; Robotic Radical Prostatectomy |
| Interventions | ; |
Prostate cancer is the most common cancer amongst men in the United Kingdom, and two common curative treatments are surgery to remove the prostate (radical prostatectomy) or radiotherapy. Both treatments can affect quality of life, mainly because of problems with erections and urinary leakage. Many men feel disappointed or regret their treatment choice because of changes in their sexual functio…
NCT07273773 — Evaluation of the Rigicon Infla10® Inflatable Penile Prosthesis (IPP) for Erectile Dysfunction
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Rigicon, Inc. |
| Enrollment | 182 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction (ED) |
| Interventions |
This study evaluates the long-term safety and effectiveness of the Rigicon Infla10® Inflatable Penile Prosthesis in patients with erectile dysfunction. The study follows patients implanted with the Rigicon Infla10® Pulse™ Dynamic Inflatable Penile Prosthesis for up to 3 years after implantation.
NCT07188064 — A Study Looking at a New Nerve Surgery to Help Men Regain Erections After Prostate Cancer Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Sir Mortimer B. Davis - Jewish General Hospital |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Erectile Dysfunction Following Radical Prostatectomy |
| Interventions |
A single arm prospective pilot trial evaluating the 1-year erectile recovery outcomes and the safety of patients undergoing a somatic to autonomic nerve grafting procedure for restoration of erectile function in patients who have lost erectile function following radical prostatectomy for prostate cancer. During this study a total of 100 patients who have persistent erectile dysfunction for more…
NCT07442396 — The Effectiveness of Exercise in the Treatment of Erectile Dysfunction and Premature Ejaculation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Uskudar University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction; Premature Ejaculation |
| Interventions | ; |
The aim is to investigate the effectiveness of exercise in the treatment of erectile dysfunction and premature ejaculation.
NCT07460960 — TRIal of STatin Therapy Effect on Androgen Status and Erectile functioN in Men
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Lomonosov Moscow State University Medical Research and Educational Center |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction Due to Arterial Disease; Atheroscleroses; Erectile Disfunction; Endothelial Dysfunction; Androgen Profile |
| Interventions | ; |
Aim. To study the effect of different intensities of statin therapy on androgen status and erectile function in men aged 40-65 years with high and very high cardiovascular risk. Additionally, to assess the association between sex hormone levels, erectile function parameters, and traditional cardiovascular risk factors, arterial stiffness, and endothelial function in this patient category.
Mate…
NCT07520916 — The Effect of Mobile-Based Perioperative Education on Urinary Incontinence and Erectile Function After Radical Prostatectomy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Giresun University |
| Enrollment | 78 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer (Post Prostatectomy); Urinary Incontinence (UI); Erectile Dysfunction Following Radical Prostatectomy |
| Interventions | ; |
This prospective randomized controlled study aims to evaluate the effect of mobile-based perioperative education on postoperative urinary incontinence and erectile function in patients undergoing radical prostatectomy. Patients scheduled for radical prostatectomy will be assigned to either an intervention group or a control group. The intervention group will receive standard care plus a structu…
NCT07601646 — A Single-Arm, Dose Escalation of an Intraurethral Alprostadil Paste for Erectile Dysfunction
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Ryan Flannigan, MD |
| Enrollment | 83 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction (ED); Erectile Dysfunctions; Erectile Function |
| Interventions |
This is a single arm dose escalation trial of a mucoadhesive intraurethral polymer suspension of alprostadil (ST-04) and will investigate the efficacy of 3 dose levels of ST-04 in adult males with a clinical diagnosis of Erectile Dysfunction (ED). This study aims to determine if ST-04, with or without sildenafil, will improve erectile function (EF) compared to baseline.
Participants in this st…
NCT07642505 — L-Citrulline and Tadalafil for Mild to Moderate Erectile Dysfunction
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Beni-Suef University |
| Enrollment | 133 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; ; |
Erectile dysfunction is a common male sexual health problem that may affect quality of life and sexual relationships. Tadalafil 5 mg once daily is an established oral treatment for erectile dysfunction. L-citrulline is an oral nitric oxide pathway supplement that may improve erectile function by increasing L-arginine availability.
This randomized trial will compare three oral treatment regimen…
Active, Not Recruiting
NCT03525262 — Prostate Oncologic Therapy While Ensuring Neurovascular Conservation (POTEN-C)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | 124 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer Adenocarcinoma |
| Interventions |
Reduction of dose to or ‘sparing’ of neurovascular structures during stereotactic ablative body radiotherapy (SAbR) for localized prostate cancer will improve retention of sexual potency, while retaining excellent oncologic control and other secondary health-related quality of life (HRQOL) endpoints.
Primary Objectives:
• To compare the decline in patient health-related quality of life (HRQOL…
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).
NCT06397612 — Efficacy of Low-dose Percutaneous Electrical Stimulation in Patients With Erectile Dysfunction.
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Camilo Jose Cela University |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Pudendal Nerve Injury; Erectile Dysfunction; Electric Stimulation |
| Interventions |
Erectile dysfunction is known as any alteration that produces a modification in the erectile response, whether it is due to organic, psychogenic or relational causes. Peripheral percutaneous nerve stimulation is performed using a needle to stimulate the peripheral nerves in such a way as to stimulate most of the area of the structure, stimulating sensory and motor nerve endings in the deeper ti…
NCT06433596 — Autologous PRP and Focal Shock Waves for Erectile Dysfunction
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Elexial Research Limited |
| Enrollment | 116 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; ; |
The goal of this clinical trial is to learn if Platelet-rich plasma (PRP) combined with Shock-wave therapy (SWT) works to treat moderate or mild to moderate erectile dysfunction. It will also learn about the safety of this combined therapy.
The main questions it aims to answer are:
- Does Combined therapy PRP + SWT improve erection in men with moderate or mild to moderate erectile dysfunction…
NCT07544537 — A Prospective Comparative Study of Autologous Bone Marrow-Derived and Adipose Tissue-Derived Mesenchymal Stem Cells Versus Platelet-Rich Plasma and Standard Therapy in Patients With Organic Erectile Dysfunction
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Scientific Medical Center, Kazakhstan |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; ; |
Erectile dysfunction (ED) is a common condition characterized by the inability to achieve or maintain an erection sufficient for satisfactory sexual activity. It can significantly affect physical health, emotional well-being, and quality of life for both patients and their partners. Standard treatment options include medications such as phosphodiesterase type 5 inhibitors, vacuum devices, intra…
NCT07479901 — Investigation of the Effect of the Atherogenic Index on the Therapeutic Response to Tadalafil in Patients With Vascular Erectile Dysfunction
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Taksim Egitim ve Arastirma Hastanesi |
| Enrollment | 132 |
| Study Type | OBSERVATIONAL |
| Conditions | Erectile Dysfunction Vascular Erectile Dysfunction Atherogenic Dyslipidemia |
This study aims to investigate the relationship between the atherogenic index of plasma (AIP) and the therapeutic response to daily tadalafil 5 mg treatment in patients diagnosed with vascular erectile dysfunction (VED). AIP is considered a marker of atherogenic dyslipidemia and subclinical atherosclerosis and is calculated using the formula log10 (triglycerides/HDL-C). Since vascular abnormali…
NCT07627477 — Impact of Depression Severity on Sexual Dysfunction
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Sohag University |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Depression; Erectile Dysfunction; Premature Ejaculation |
Assess the relationship and the prevalence…" “To determine the prevalence of erectile dysfunction and premature ejaculation among depressed male patients and evaluate their association with depression severity.”
NCT07676617 — Satisfaction of Patients With Erectile Dysfunction With the Use of Sildenafil Oral Suspension Compared to Orodispersible Tablets
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico |
| Enrollment | 55 |
| Study Type | OBSERVATIONAL |
| Conditions | Erectile Dysfunction; Erectile Dysfunction (ED) |
| Interventions |
The goal of this observational retrospective study is to to evaluate treatment satisfaction with sildenafil oral suspension in patients with mild-to-moderate ED who were previously taking orodispersible sildenafil.
The secondary objective is to evaluate the efficacy and side effects of therapy with sildenafil oral suspension compared to orodispersible sildenafil.
Patients who took sildenafil …
Not Yet Recruiting
NCT07048314 — Stem Cells for Erectile Dysfunction Post RALP
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | The Methodist Hospital Research Institute |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction; Prostate Cancer |
| Interventions | ; ; |
This is a phase 1/2 single center, pilot study to assess safety and efficacy of allogeneic adipose-derived mesenchymal stem cells (HB-adMSCs) and to evaluate the timing and combination effects of active treatment versus placebo in promoting the recovery of erectile function in patients undergoing radical retropubic prostatectomy (RALP) of localized prostate cancer.
NCT07460726 — PRIAPUS-PCa Study: Stereotactic Body Radiation Therapy (SBRT) and Androgen Deprivation Therapy (ADT) Impact on Sexual Function on Men With Unfavorable Intermediate Risk Prostate Cancer
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | CancerCare Manitoba |
| Enrollment | 130 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer (Adenocarcinoma); Erectile Abnormalities; Sexual Dysfunction Male |
| Interventions |
This study looks at how combined radiation and hormone therapy affects sexual function in men with a specific type of prostate cancer, before and after treatment.
NCT07576335 — Multimodal Prehabilitation and Rehabilitation for Men Undergoing Robot-Assisted Radical Prostatectomy
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Surgical Outcomes Research Centre (SOuRCe) |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction Following Radical Prostatectomy; Prostate Cancer; Urinary Incontinence Following Surgical Procedure |
| Interventions | ; ; |
Prostate cancer is the most common cancer in Australian men. Robot-assisted radical prostatectomy (RARP) - surgical removal of the prostate - is a standard treatment, but it frequently causes erectile dysfunction (ED) and urinary incontinence that can persist for years and significantly affect quality of life.
This trial (ROBOPREP) will test whether a multimodal program of prehabilitation (bef…
NCT07537855 — Efficacy of Intracavernosal Xeomin With Tadalafil for Mild-Moderate Erectile Dysfunction
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Northwestern University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; ; |
Erectile dysfunction (ED) affects approximately 30 million men in the United States and is associated with factors such as aging, smoking, diabetes, hypertension, obesity, and sedentary lifestyle. ED can also negatively impact the quality of life of patients and their partners. Treatment decisions are typically made jointly between patients and their urologists, often starting with less invasiv…
NCT07604194 — Embolosclerotherapy Versus Deep Dorsal Vein Revascularization in Venogenic Erectile Dysfunction
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Mansoura University Hospital |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction Due to Venous Disorder; Erectile Dysfunction (ED) |
| Interventions | ; |
Venous leakage is one of the causes of erectile dysfunction and can be managed using different treatment modalities, including surgical ligation and percutaneous embolization. This randomized clinical trial aims to evaluate and compare the efficacy, durability, safety, side effects, and complications of two treatment procedures-embolosclerotherapy of the periprostatic plexus and deep dorsal vei…
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…
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 …
NCT07687173 — Assessment of Effectiveness of Pelvic Floor Muscle Training With Biofeedback in Male With Hypogonadism and Erectile Dysfunction
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Poznan University of Physical Education |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Disfunction; Hypogonadal Males; Functional Hypogonadism; Pelvic Floor Muscle Exercise; Biofeedback Training |
| Interventions | ; |
The goal of this clinical trial is to learn if Pelvic Floor Muscle Training (PFMT) with biofeedback works to treat Erectile Disorders (ED) in males with Functional Hipogonadism. The main hypothesis is:
1. Biofeedback-assisted Pelvic Floor Muscle Training will cause greater improvement in pelvic floor muscle strength and endurance and sexual life than in group without biofeedback and control g…
NCT07636161 — PLEASURE (Pleasing Lovers, Efficacy, Arousal, Satisfaction, and Uptake Research on Eroxon)
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | University of Miami |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes; Type 2 Diabetes (T2DM) |
| Interventions | ; |
The purpose of this research study is to look at whether Eroxon® gel when used together with tadalafil, may help improve erectile function in men ages 18 to 40 who have type 2 diabetes.
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…
NCT07451808 — Male Pelvic Floor Muscle Rehabilitation Exercises
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Dream Video LLC |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction; Urinary Incontinence; Premature Ejaculation |
| Interventions |
Phase I
G128 Study Objective
The ischiocavernosus (IC) and bulbospongiosus (BS) muscles are vital components of the superficial perineal layer, serving as the foundation for male sexual health and performance. These muscles play a primary role in achieving and maintaining erections by compressing the veins to trap blood within the erectile tissues. Furthermore, they are responsible for the rh…
Enrolling by Invitation
NCT04200937 — IT Matters: The Erectile Restoration Registry
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Boston Scientific Corporation |
| Enrollment | 450 |
| Study Type | OBSERVATIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; ; |
The objective of the It MATTERS registry is to collect Real-World Data (RWD) to monitor the safe and effective use of commercially available Boston Scientific Corporation (BSC) penile prostheses
NCT07469345 — Bruxism, Pelvic Pain, Erectile Dysfunction, and Anxiety in Young Adult Men
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Akdeniz University |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Bruxism; Pelvic Pain; Myofascial Pain - Dysfunction Syndrome of TMJ; Myofascial Pain Dysfunction Syndrome |
| Interventions |
Bruxism is a parafunctional activity characterized by clenching or grinding of the teeth during wakefulness or sleep. Increasing evidence suggests that bruxism is not only related to orofacial structures but may also be associated with broader musculoskeletal and psychosocial conditions. Emerging literature indicates that central sensitization, stress, and anxiety may contribute to both bruxism…
Completed Trials
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.
NCT03596047 — Radial Shockwave Therapy for Erectile Dysfunction
| Status | Completed |
| Phase | N/A |
| Sponsor | Boston Medical Group |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; |
Objective: To evaluate the efficacy and safety of radial shock waves for the treatment of erectile dysfunction [ED].
Patients and methods: Randomized, double-blind clinical trial. The study will include patients of legal age with diagnosis of ED and score on the International Index of Erectile Function [IIEF-EF] scale between 11 and 21 points, who voluntarily decide to participate and sign…
NCT07453628 — Association of Erectile Dysfunction With Neuropathic Pain, Disease Activity, and Functional Status in Male Patients With Axial Spondyloarthritis: A Cross-Sectional Observational Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Altuğ Güner |
| Enrollment | 90 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankylosing Spondylitis; Sexual Dysfunction |
| Interventions | ; ; |
tudy Description Definitions Use this module to describe the study protocol.
- Required
- § Required if Study Start Date is on or after January 18, 2017 [*] Conditionally required
Brief Summary
*
Use these resources to provide understandable information about this study to patients, families, and health care providers:
Plain language checklist for Brief Summary Template for Brief Summa…
NCT05048667 — Shockwave Therapy and Platelet Rich Plasma for the Treatment of Erectile Dysfunction
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | University of Miami |
| Enrollment | 59 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; ; |
The purpose of this research study is to evaluate whether the combination of Shock Wave Therapy (SWT) with Platelet Rich Plasma (PRP) is synergistic and can reverse the pathology of microvascular Erectile Dysfunction (ED) and enhance erectile function by improving vasodilation, and endothelial function
NCT05673005 — MED3000 Topical Gel for On-Demand Treatment of Post-Radical Prostatectomy Erectile Dysfunction
| Status | Completed |
| Phase | N/A |
| Sponsor | Brigham and Women’s Hospital |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction Following Radical Prostatectomy |
| Interventions |
The investigators are doing this research to evaluate the efficacy and safety of topical MED3000 therapy in men with persistent erectile dysfunction 1.5 to 4 years following radical prostatectomy surgery.
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…
NCT07574268 — Efficacy of Transcutaneous Electrical Neural Stimulation and Tadalafil in Men With Erectile Dysfunction: A Randomized, Double-Blind, Bi-centric, Placebo- and Sham-Controlled Trial
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Menoufia University |
| Enrollment | 185 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction |
| Interventions | ; ; |
Organic erectile failure is thought to be caused predominantly by neurogenic or vascular disorders. Venoocclusive dysfunction of the corpora cavernosa induces erectile dysfunction in 20-30% and appears clinically by premature erection loss.
The increased venous outflow from the corpora cavernosa can be illustrated as a so called ‘venous leakage’ by cavernosography being responsible for the the…
NCT06501144 — Real-world Longitudinal Follow-up Study of a Digital Health Application in Erectile Dysfunction
| Status | Completed |
| Phase | N/A |
| Sponsor | Kranus Health GmbH |
| Enrollment | 317 |
| Study Type | OBSERVATIONAL |
| Conditions | Erectile Dysfunction; Sexual Dysfunction |
The goal of this observational study is to assess the long-term effectiveness of a digital health application for treating erectile dysfunction in men aged 18 and older. The main questions it aims to answer are:
- Will participants maintain an improvement of their erectile function, that means maintain an improvement of at least 3 points in the IIEF-5 score at 3 months post-therapy?
- How does…
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…
NCT07563647 — Association Between Diastolic Dysfunction and Erectile Dysfunction and the Effect of Tadalafil and SGLT2 Inhibitors on Them in Men With Metabolic Syndrome
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Kafrelsheikh University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Erectile Dysfunction; Left Ventricular Diastolic Dysfunction; Metabolic Syndrome |
| Interventions | ; ; |
Metabolic syndrome is associated with an increased risk of cardiovascular disease and is commonly accompanied by erectile dysfunction and subclinical cardiac dysfunction. Erectile dysfunction and left ventricular diastolic dysfunction may share common underlying mechanisms, including endothelial dysfunction and microvascular impairment.
This study aims to investigate the association between er…
NCT07293156 — Impact of Pilates Exercises on Diabetic Erectile Dysfunction.
| Status | Completed |
| Phase | N/A |
| Sponsor | Benha University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabete Mellitus; Erectile Dysfunction Associated With Type 2 Diabetes Mellitus; Pilates Exercise; Pelvic Floor Muscle Exercise |
| Interventions | ; ; |
Erectile dysfunction (ED) has a prevalence of 52.5% in diabetic male patients, as described in a meta-analysis of 145 studies, including 88,577 men with type 1 and type 2 diabetes.
In men, ED can cause sexual dissatisfaction and distress, unsatisfactory relationships, and marital tension