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NCT00177125 · ClinicalTrials.gov registry record · Phase 3
Evaluating the Effect of the VCD on Erectile Function and Penile Length Post RRP
A Phase 3 study, sponsored by University of Minnesota.
- Completed
- Registry status
- Phase 3
- Development phase
- 220
- Enrollment target
NCT00177125: Completed Phase 3 study, sponsored by University of Minnesota.
NCT00177125 is a Phase 3 study that has completed, run by University of Minnesota. The registered enrollment target is 220 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00177125, a Phase 3 study, has completed, sponsored by University of Minnesota.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 220 participants
- Enrollment target
Study Summary
The purpose of this study is to perform a randomized prospective study to evaluate whether the vacuum erection device facilitates an earlier return of erectile function post radical prostatectomy. A secondary measure will be to evaluate if the vacuum erection device can help prevent penile shortening.
Interventions
- DEVICE ErectAid
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 220 participants |
| Start Date | 2004-01 |
| Est. Completion | 2004-01 |
| Phase | Phase 3 |
What the finished NCT00177125 record still lists
NCT00177125 is an interventional study that assigns participants to a tested intervention. The registered 220 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower).
The record links to 0 conditions, and to 1 intervention - of which ErectAid is the first listed.
NCT00177125 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00177125 about?
NCT00177125 is a clinical study titled "Evaluating the Effect of the VCD on Erectile Function and Penile Length Post RRP". The purpose of this study is to perform a randomized prospective study to evaluate whether the vacuum erection device facilitates an earlier return of erectile function post radical prostatectomy. A secondary measure will be to evaluate if the vacuum erection device can help prevent penile shortenin...
What is the current status of trial NCT00177125?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 220 participants. The study started on 2004-01. Estimated completion is 2004-01.
What interventions are being tested in trial NCT00177125?
The interventions under investigation include: ErectAid (DEVICE).
Who is sponsoring clinical trial NCT00177125?
This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00177125's enrollment target sits among peer trials
220 1318th of 2000 higher than 672 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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