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NCT05128682 · ClinicalTrials.gov registry record · NA
Acute Pudendal Nerve Stimulation On Leak Point Pressure In Women Urodynamic Early Feasibility Study
A NA study, sponsored by Corewell Health East.
- Terminated
- Registry status
- NA
- Development phase
- 4
- Enrollment target
NCT05128682 is a NA study that was terminated before completion, run by Corewell Health East. The registered enrollment target is 4 participants.
The verdict
NCT05128682, a NA study, was terminated before completion, sponsored by Corewell Health East.
- TERMINATED
- Registry status
- NA
- Development phase
- 4 participants
- Enrollment target
Study Summary
The purpose of this study is tp evaluate the changes in stress induced Urethral Leak Point Pressures (LPP) and other urodynamic measurements in response to acute pudendal nerve stimulation (PNS) in patients with a pre-existing implanted urological neurostimulator stimulating the pudendal nerve.
Interventions
- DIAGNOSTIC_TEST Urodynamic testing with and without pudendal nerve stimulation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4 participants |
| Start Date | 2022-05-24 |
| Est. Completion | 2022-09-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05128682
The ClinicalTrials.gov registry entry for NCT05128682 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Corewell Health East, which has 106 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Urodynamic testing with and without pudendal nerve stimulation is the first listed.
NCT05128682 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05128682 about?
NCT05128682 is a clinical study titled "Acute Pudendal Nerve Stimulation On Leak Point Pressure In Women Urodynamic Early Feasibility Study". The purpose of this study is tp evaluate the changes in stress induced Urethral Leak Point Pressures (LPP) and other urodynamic measurements in response to acute pudendal nerve stimulation (PNS) in patients with a pre-existing implanted urological neurostimulator stimulating the pudendal nerve.
What is the current status of trial NCT05128682?
This trial is currently terminated. It is a NA study. The enrollment target is 4 participants. The study started on 2022-05-24. Estimated completion is 2022-09-07.
What interventions are being tested in trial NCT05128682?
The interventions under investigation include: Urodynamic testing with and without pudendal nerve stimulation (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT05128682?
This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.
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