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

Evaluating the Effect of the Vacuum Constriction Device on Erectile Function and Penile Length Post Radical Retropubic Prostatectomy

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00177125
Enrollment
220
Registered
2005-09-15
Start date
2004-01-31
Completion date
2004-01-31
Last updated
2012-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostatectomy, Prostatic Neoplasms

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 secondary measure will be to evaluate if the vacuum erection device can help prevent penile shortening.

Interventions

DEVICEErectAid

Sponsors

Endocare, Inc.
CollaboratorINDUSTRY
Manoj, Monga, M.D.
CollaboratorINDIV
University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing a radical prostatectomy for prostate cancer who are able to attain a partial or full erection preoperatively and are sexually active.

Exclusion criteria

* 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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026