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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: Clinical Trial NA study, sponsored by Corewell Health East.
NCT05128682 is a NA study that was terminated before completion, run by Corewell Health East. The registered enrollment target is 4 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
PNS final settings including: pulse amplitude, measured in mA, when subject first verbalizes sensation. Pulse amplitude is the amplitude of the electric pulses; measured in Milliamps (mA). This is a setting present on the neuromodulation device, it is not calculated.
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 |
Why NCT05128682 stopped before completion
NCT05128682 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
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 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05128682's enrollment target sits among peer trials
4 1996th of 2000 higher than 5 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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