Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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 is a Phase 3 study that has completed, run by University of Minnesota. The registered enrollment target is 220 participants.
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00177125
The ClinicalTrials.gov registry entry for NCT00177125 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 220 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which ErectAid is the first listed.
NCT00177125 reports 0 study locations.
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
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.