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NCT07053826 · ClinicalTrials.gov registry record · NA
Penile Lengthening Pre-Penile Prosthesis Implantation
A NA study of Erectile Dysfunction, sponsored by University of Pittsburgh.
- Recruiting
- Registry status
- NA
- Development phase
- 48
- Enrollment target
- 1
- Study location
NCT07053826 is a NA study of Erectile Dysfunction that is actively recruiting participants, run by University of Pittsburgh. The registered enrollment target is 48 participants, below the 230-participant average among 33 other Erectile Dysfunction trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07053826, a NA study of Erectile Dysfunction, is actively recruiting participants, sponsored by University of Pittsburgh.
- RECRUITING
- Registry status
- NA
- Development phase
- 48 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this study is to determine whether or not the use of a penile traction therapy device known as RestoreX prior to implantation of a penile prosthesis can increase the length of the implant used during surgery. The device used in this study is commercially available and has been used successfully to facilitate penile lengthening in patients with diabetes and after a certain type of prostate surgery. Use of the device has not been shown to have any detrimental effects on sexual or overall health.
Conditions Studied
Interventions
- DEVICE Penile Traction Device
- PROCEDURE Inflatable Penile Prosthesis Implantation
Study Locations (1)
Pennsylvania
- UPMC Mercy Hospital, Urology - Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2025-08-26 |
| Est. Completion | 2027-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07053826
The ClinicalTrials.gov registry entry for NCT07053826 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 48 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 (79% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Erectile Dysfunction appearing as the primary indexed condition, and to 2 interventions - of which Penile Traction Device is the first listed.
NCT07053826 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT07053826 about?
NCT07053826 is a clinical study titled "Penile Lengthening Pre-Penile Prosthesis Implantation". The goal of this study is to determine whether or not the use of a penile traction therapy device known as RestoreX prior to implantation of a penile prosthesis can increase the length of the implant used during surgery. The device used in this study is commercially available and has been used succe...
What is the current status of trial NCT07053826?
This trial is currently recruiting. It is a NA study. The enrollment target is 48 participants. The study started on 2025-08-26. Estimated completion is 2027-02.
What conditions does trial NCT07053826 study?
This clinical trial studies the following conditions: Erectile Dysfunction.
What interventions are being tested in trial NCT07053826?
The interventions under investigation include: Penile Traction Device (DEVICE), Inflatable Penile Prosthesis Implantation (PROCEDURE).
Who is sponsoring clinical trial NCT07053826?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07053826 being conducted?
This trial has 1 study location across Pennsylvania. 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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