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NCT05210738 · ClinicalTrials.gov registry record
Single-incision Sling vs Urethral Bulking During Prolapse Surgery for Occult Stress Incontinence
A clinical trial of Stress Incontinence Female, sponsored by The Christ Hospital.
- Completed
- Registry status
- 60
- Enrollment target
- 1
- Study location
NCT05210738: Completed study of Stress Incontinence Female, sponsored by The Christ Hospital.
NCT05210738 is a study of Stress Incontinence Female that has completed, run by The Christ Hospital. The registered enrollment target is 60 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05210738, a study of Stress Incontinence Female, has completed, sponsored by The Christ Hospital.
- COMPLETED
- Registry status
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
The aim is to compare outcomes of two different procedures to prevent occult stress urinary incontinence (SUI) in patients who are having pelvic organ prolapse surgeries
Conditions Studied
Interventions
- DEVICE Single incision sling
- DRUG Bulkamid bulking agent
Study Locations (1)
Ohio
- The Christ Hospital - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2019-01-01 |
| Est. Completion | 2021-06-01 |
What the finished NCT05210738 record still lists
NCT05210738 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 60 participants, a relatively small participant target.
The record links to 1 condition, with Stress Incontinence Female appearing as the primary indexed condition, and to 2 interventions - of which Single incision sling is the first listed.
NCT05210738 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT05210738 about?
NCT05210738 is a clinical study titled "Single-incision Sling vs Urethral Bulking During Prolapse Surgery for Occult Stress Incontinence". The aim is to compare outcomes of two different procedures to prevent occult stress urinary incontinence (SUI) in patients who are having pelvic organ prolapse surgeries
What is the current status of trial NCT05210738?
This trial is currently completed. The enrollment target is 60 participants. The study started on 2019-01-01. Estimated completion is 2021-06-01.
What conditions does trial NCT05210738 study?
This clinical trial studies the following conditions: Stress Incontinence Female.
What interventions are being tested in trial NCT05210738?
The interventions under investigation include: Single incision sling (DEVICE), Bulkamid bulking agent (DRUG).
Who is sponsoring clinical trial NCT05210738?
This trial is sponsored by The Christ Hospital, which has 13 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05210738 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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