Status:
COMPLETED
Evaluating the Effect of the VCD on Erectile Function and Penile Length Post RRP
Lead Sponsor:
University of Minnesota
Collaborating Sponsors:
Endocare, Inc.
Manoj, Monga, M.D.
Conditions:
Prostatic Neoplasms
Prostatectomy
Eligibility:
MALE
18+ years
Phase:
PHASE3
Brief 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 s...
Eligibility Criteria
Inclusion
- Patients undergoing a radical prostatectomy for prostate cancer who are able to attain a partial or full erection preoperatively and are sexually active.
Exclusion
- Patients on anticoagulation therapy and those with bleeding diatheses
- Insufficient manual dexterity of patient or spouse
- IIEF(International Index of Erectile Function) at baseline \< 11, indicating severe erectile dysfunction
Key Trial Info
Start Date :
January 1 2004
Trial Type :
INTERVENTIONAL
End Date :
January 1 2004
Estimated Enrollment :
220 Patients enrolled
Trial Details
Trial ID
NCT00177125
Start Date
January 1 2004
End Date
January 1 2004
Last Update
February 6 2012
Active Locations (2)
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1
VAMC Minneapolis
Minneapolis, Minnesota, United States, 55417
2
University of Minnesota
Minneapolis, Minnesota, United States, 55455