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NCT03048682 · ClinicalTrials.gov registry record · NA
Timing of Repeat Voiding Trials After Outpatient Pelvic Floor Surgery
A NA study of Surgery and Pelvic Organ Prolapse, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 64
- Enrollment target
- 2
- Study locations
NCT03048682 is a NA study of Surgery and Pelvic Organ Prolapse that has completed, run by The Cleveland Clinic. The registered enrollment target is 64 participants, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT03048682, a NA study of Surgery and Pelvic Organ Prolapse, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 64 participants
- Enrollment target
- 2
- Study locations
Study Summary
This study is a randomized controlled trial designed to assess the rate of failure of voiding trials in the early and late post-operative period within patients who underwent outpatient pelvic floor surgery that failed initial same day voiding trials.
Conditions Studied
Interventions
- DEVICE Foley catheter - Early Voiding Trial
- DEVICE Foley catheter - Late Voiding Trial
Study Locations (2)
Florida
- Cleveland Clinic Florida - Weston
North Carolina
- Wake Forest Baptist Health - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2017-01-05 |
| Est. Completion | 2019-11-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03048682
The ClinicalTrials.gov registry entry for NCT03048682 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Surgery appearing as the primary indexed condition, and to 2 interventions - of which Foley catheter - Early Voiding Trial is the first listed.
NCT03048682 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, North Carolina.
Frequently Asked Questions
What is clinical trial NCT03048682 about?
NCT03048682 is a clinical study titled "Timing of Repeat Voiding Trials After Outpatient Pelvic Floor Surgery". This study is a randomized controlled trial designed to assess the rate of failure of voiding trials in the early and late post-operative period within patients who underwent outpatient pelvic floor surgery that failed initial same day voiding trials.
What is the current status of trial NCT03048682?
This trial is currently completed. It is a NA study. The enrollment target is 64 participants. The study started on 2017-01-05. Estimated completion is 2019-11-30.
What conditions does trial NCT03048682 study?
This clinical trial studies the following conditions: Surgery, Pelvic Organ Prolapse, Urinary Incontinence,Stress.
What interventions are being tested in trial NCT03048682?
The interventions under investigation include: Foley catheter - Early Voiding Trial (DEVICE), Foley catheter - Late Voiding Trial (DEVICE).
Who is sponsoring clinical trial NCT03048682?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03048682 being conducted?
This trial has 2 study locations across Florida, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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