Trials / Completed
CompletedNCT05673005
MED3000 Topical Gel for On-Demand Treatment of Post-Radical Prostatectomy Erectile Dysfunction
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Brigham and Women's Hospital · Academic / Other
- Sex
- All
- Age
- 40 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
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.
Detailed description
MED3000 is a topical gel that has been developed to treat patients with erectile dysfunction. The investigators postulate that on demand treatment with MED3000 can improve on-demand erectile function among men status-post radical prostatectomy, allowing for some endogenous cavernosal nerve function recovery for 1.5 to 4 years post-surgery among men with normal baseline pre-surgical erectile function.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | MED3000 topical gel | Topical gel that has been shown to improve erectile dysfunction when used as needed. |
Timeline
- Start date
- 2023-04-01
- Primary completion
- 2024-07-24
- Completion
- 2024-08-09
- First posted
- 2023-01-05
- Last updated
- 2026-03-11
- Results posted
- 2025-12-30
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05673005. Inclusion in this directory is not an endorsement.