At a glance

ClinicalIndex Comparison Record

N/ACompleted· 40 enrolled

Drug / intervention

Inflatable Penile Prosthesisdevice

Likely dose

Not stated in record

Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00731666

NCT00731666N/ACompleted

Compare CT.gov

Prospective, Non-randomized, Multi-center Clinical Trial to Assess the Effectiveness of the Coloplast Titan® IPP at Maintaining or Increasing Penile Length After Implantation

Coloplast A/S·interventional·Posted Aug 11, 2008·Updated Nov 28, 2013

In Brief

A clinical study evaluating Inflatable Penile Prosthesis for Erectile Dysfunction. Completed, enrolled 40 participants across 3 sites.

Detailed Summary

This study is designed to assess the effectiveness of the Coloplast Titan® Inflatable Penile Prosthesis (IPP) at maintaining or increasing penile length after implantation of the device. It will incorporate a modified method of cylinder sizing during implantation and a max-inflate technique after implantation.

Study Details

Study Typeinterventional

Allocation--

Masking--

Primary Purpose--

ConditionsErectile Dysfunction

CountriesUnited States

Collaborators--

Timeline

N/ACompletedFinished

20082009201020112012201320142015201620172018201920202021202220232024202520262027

Enrollment StartDec 2007

First PostedAug 2008

Primary CompletionMay 2010

Study CompletionMay 2011

TodayJul 2026

First PostedAug 11, 2008

Enrollment StartDec 1, 2007

Primary CompletionMay 1, 2010

Study CompletionMay 1, 2011

TodayJul 2, 2026

Enrollment to primary: 2.4 yearsPosted 17.9 years ago

Interventions

Inflatable Penile Prosthesisdevice

Hydraulic system designed to be surgically implanted into the penis for the management of erectile dysfunction. The implant provides the participant with voluntary control over the erect and flaccid states of the penis.