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NCT05900570 · ClinicalTrials.gov registry record · NA
Effect of Peri-Urethral Stimulation on Intra-Urethral Pressure
A NA study of Stress Urinary Incontinence, sponsored by Corewell Health East.
- Recruiting
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT05900570 is a NA study of Stress Urinary Incontinence that is actively recruiting participants, run by Corewell Health East. The registered enrollment target is 20 participants, below the 162-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05900570, a NA study of Stress Urinary Incontinence, is actively recruiting participants, sponsored by Corewell Health East.
- RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this early feasibility prospective study is to gain initial understanding of the effect of acute peri-urethral neurostimulation on the perineal nerves on intra-urethral pressure.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Urodynamic testing with and without pudendal nerve stimulation
Study Locations (1)
Michigan
- Corewell Health William Beaumont University Hospital - Royal Oak
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2024-02-26 |
| Est. Completion | 2027-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05900570
The ClinicalTrials.gov registry entry for NCT05900570 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 162-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (88% lower). The listed sponsor is Corewell Health East, which has 106 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Stress Urinary Incontinence appearing as the primary indexed condition, and to 1 intervention - of which Urodynamic testing with and without pudendal nerve stimulation is the first listed.
NCT05900570 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.
Frequently Asked Questions
What is clinical trial NCT05900570 about?
NCT05900570 is a clinical study titled "Effect of Peri-Urethral Stimulation on Intra-Urethral Pressure". The purpose of this early feasibility prospective study is to gain initial understanding of the effect of acute peri-urethral neurostimulation on the perineal nerves on intra-urethral pressure.
What is the current status of trial NCT05900570?
This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2024-02-26. Estimated completion is 2027-01.
What conditions does trial NCT05900570 study?
This clinical trial studies the following conditions: Stress Urinary Incontinence.
What interventions are being tested in trial NCT05900570?
The interventions under investigation include: Urodynamic testing with and without pudendal nerve stimulation (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT05900570?
This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05900570 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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