Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01262833 · ClinicalTrials.gov registry record
Pudendal Assessment in Erectile Dysfunction
A clinical trial, sponsored by University of Pennsylvania.
- Terminated
- Registry status
- 10
- Enrollment target
NCT01262833: Clinical Trial study, sponsored by University of Pennsylvania.
NCT01262833 is a clinical trial that was terminated before completion, run by University of Pennsylvania. The registered enrollment target is 10 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01262833 was terminated before completion, sponsored by University of Pennsylvania.
- TERMINATED
- Registry status
- 10 participants
- Enrollment target
Study Summary
The study will address the role of internal pudendal artery disease in erectile dysfunction (ED), and whether it might eventually be amenable to intervention with stenting. There is currently a small trial investigating the potential benefit of stenting for erectile dysfunction, but the relationship between pelvic arterial stenoses and erectile dysfunction is not yet proven. The investigators intend to perform angiography on patients both with and without erectile dysfunction, to see whether internal pudendal artery disease is more common in the population with erectile dysfunction. In addition to angiography, stenoses will be examined using fractional flow reserve. The degree of internal pudendal artery disease will then be correlated with the degree of erectile dysfunction using a validated questionnaire, the International Index of Erectile Function (IIEF). Patients will then complete IIEF questionnaires for 5 years to assess the relationship between internal pudendal artery disease and progression of erectile dysfunction.
Primary Outcome
The primary exposure will be hemodynamically significant internal pudendal artery stenoses as a predictor of erectile dysfunction
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2010-09 |
| Est. Completion | 2013-09 |
Why NCT01262833 stopped before completion
NCT01262833 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 10 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT01262833 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01262833 about?
NCT01262833 is a clinical study titled "Pudendal Assessment in Erectile Dysfunction". The study will address the role of internal pudendal artery disease in erectile dysfunction (ED), and whether it might eventually be amenable to intervention with stenting. There is currently a small trial investigating the potential benefit of stenting for erectile dysfunction, but the relationship...
What is the current status of trial NCT01262833?
This trial is currently terminated. The enrollment target is 10 participants. The study started on 2010-09. Estimated completion is 2013-09.
Who is sponsoring clinical trial NCT01262833?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT00623389 · 10 participants · NA
Evaluation of an Advanced Lower Extremity Neuroprostheses
- NCT01241864 · 10 participants · Phase 2
Islet Transplantation in Type 1 Diabetic Kidney Allograft
- NCT01293214 · 10 participants · NA
Vascularized Composite Allotransplantation for Multiple Extremity Amputations
- NCT01474148 · 10 participants · NA
A Neuroprosthesis for Seated Posture and Balance
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia