MedTrace Logo

Evaluating the Effect of the VCD on Erectile Function and Penile Length Post RRP

NCT00177125 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 220

Last updated 2012-02-06

No results posted yet for this 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.

Conditions

  • Prostatic Neoplasms
  • Prostatectomy

Interventions

DEVICE

ErectAid

Sponsors & Collaborators

Principal Investigators

  • Manoj Monga, MD · University of Minnesota and VAMC Minneapolis

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-01-31
Primary Completion
2004-01-31
Completion
2004-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00177125 on ClinicalTrials.gov