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NCT04826939 · ClinicalTrials.gov registry record · NA
Intravaginal Devices for Pelvic Floor Motion
A NA study, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 30
- Enrollment target
NCT04826939 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 30 participants.
The verdict
NCT04826939, a NA study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
Study Summary
The leva and PFDx devices accurately reflect pelvic floor motion consistent with TPUS evaluation. During a voluntary PFM contraction, the change in angle from a position of rest to maximal effort that is detected by each device is positively correlated with TPUS measurements and Modified Oxford scores.
Interventions
- DEVICE PFDx device and leva device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2021-03-25 |
| Est. Completion | 2022-09-26 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04826939
The ClinicalTrials.gov registry entry for NCT04826939 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which PFDx device and leva device is the first listed.
NCT04826939 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04826939 about?
NCT04826939 is a clinical study titled "Intravaginal Devices for Pelvic Floor Motion". The leva and PFDx devices accurately reflect pelvic floor motion consistent with TPUS evaluation. During a voluntary PFM contraction, the change in angle from a position of rest to maximal effort that is detected by each device is positively correlated with TPUS measurements and Modified Oxford scor...
What is the current status of trial NCT04826939?
This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2021-03-25. Estimated completion is 2022-09-26.
What interventions are being tested in trial NCT04826939?
The interventions under investigation include: PFDx device and leva device (DEVICE).
Who is sponsoring clinical trial NCT04826939?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
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