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NCT03969368 · ClinicalTrials.gov registry record · NA
rPMS Compared With Pelvic Floor Exercises for Treatment of Urinary Incontinence
A NA study, sponsored by BTL Industries.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT03969368 is a NA study that has completed, run by BTL Industries. The registered enrollment target is 60 participants.
The verdict
NCT03969368, a NA study, has completed, sponsored by BTL Industries.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
This study will compare the clinical efficacy and safety between rPMS device and pelvic floor exercises for the treatment of urinary incontinence. The subjects will be enrolled and assigned into two study groups - active and control group. Subjects will be required to complete six (6) treatment visits and five follow-up visits - 1, 3, 6, 9 and 12 months after the final treatment.
Interventions
- DEVICE rPMS device
- PROCEDURE Pelvic floor muscle training
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2019-06-01 |
| Est. Completion | 2022-06-23 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03969368
The ClinicalTrials.gov registry entry for NCT03969368 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BTL Industries, which has 40 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which rPMS device is the first listed.
NCT03969368 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03969368 about?
NCT03969368 is a clinical study titled "rPMS Compared With Pelvic Floor Exercises for Treatment of Urinary Incontinence". This study will compare the clinical efficacy and safety between rPMS device and pelvic floor exercises for the treatment of urinary incontinence. The subjects will be enrolled and assigned into two study groups - active and control group. Subjects will be required to complete six (6) treatment visi...
What is the current status of trial NCT03969368?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2019-06-01. Estimated completion is 2022-06-23.
What interventions are being tested in trial NCT03969368?
The interventions under investigation include: rPMS device (DEVICE), Pelvic floor muscle training (PROCEDURE).
Who is sponsoring clinical trial NCT03969368?
This trial is sponsored by BTL Industries, which has 40 total clinical trials registered on ClinicalTrials.gov.
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