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NCT00731666 · ClinicalTrials.gov registry record · NA
Evaluation of the Coloplast Titan® IPP for Maintaining Penile Length While Treating Erectile Dysfunction (ED)
A NA study of Erectile Dysfunction, sponsored by Coloplast A/S.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
- 3
- Study locations
NCT00731666 is a NA study of Erectile Dysfunction that has completed, run by Coloplast A/S. The registered enrollment target is 40 participants, below the 230-participant average among 33 other Erectile Dysfunction trials with a reported enrollment target (83% lower). The trial reports 3 study locations across 3 states.
The verdict
NCT00731666, a NA study of Erectile Dysfunction, has completed, sponsored by Coloplast A/S.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
- 3
- Study locations
Study 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.
Conditions Studied
Interventions
- DEVICE Inflatable Penile Prosthesis
Study Locations (3)
Florida
- James A Haley VA - Tampa
Louisiana
- Regional Urology, LLC - Shreveport
Texas
- University of Texas Health Science Center at Houston - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2007-12 |
| Est. Completion | 2011-05 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00731666
The ClinicalTrials.gov registry entry for NCT00731666 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 230-participant average among 33 other Erectile Dysfunction trials with a reported enrollment target (83% lower). The listed sponsor is Coloplast A/S, which has 21 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Erectile Dysfunction appearing as the primary indexed condition, and to 1 intervention - of which Inflatable Penile Prosthesis is the first listed.
NCT00731666 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Florida, Louisiana, Texas.
Frequently Asked Questions
What is clinical trial NCT00731666 about?
NCT00731666 is a clinical study titled "Evaluation of the Coloplast Titan® IPP for Maintaining Penile Length While Treating Erectile Dysfunction (ED)". 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 im...
What is the current status of trial NCT00731666?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2007-12. Estimated completion is 2011-05.
What conditions does trial NCT00731666 study?
This clinical trial studies the following conditions: Erectile Dysfunction.
What interventions are being tested in trial NCT00731666?
The interventions under investigation include: Inflatable Penile Prosthesis (DEVICE).
Who is sponsoring clinical trial NCT00731666?
This trial is sponsored by Coloplast A/S, which has 21 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00731666 being conducted?
This trial has 3 study locations across Florida, Louisiana, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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