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NCT03536819 · ClinicalTrials.gov registry record · NA
RF Rejuvenation for Pelvic Floor and Vagina
A NA study, sponsored by InMode MD.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT03536819: Completed NA study, sponsored by InMode MD.
NCT03536819 is a NA study that has completed, run by InMode MD. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03536819, a NA study, has completed, sponsored by InMode MD.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
Evaluation of efficacy and safety of the Votiva RF system with the Forma V handpiece for vaginal treatments.
Primary Outcome
There is no signal normalization, this measurement tool is used to measure change in Pelvic Floor Muscle function. Pelvic floor muscle Contractions amplitude are measured in mV (microvolt) 1\. Peak internal Pelvic Floor Contractions (steadily higher scores demonstrate improvement)
Interventions
- DEVICE Votiva
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2017-11-17 |
| Est. Completion | 2018-12-31 |
| Phase | NA |
What the finished NCT03536819 record still lists
NCT03536819 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Votiva is the first listed.
NCT03536819 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03536819 about?
NCT03536819 is a clinical study titled "RF Rejuvenation for Pelvic Floor and Vagina". Evaluation of efficacy and safety of the Votiva RF system with the Forma V handpiece for vaginal treatments.
What is the current status of trial NCT03536819?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2017-11-17. Estimated completion is 2018-12-31.
What interventions are being tested in trial NCT03536819?
The interventions under investigation include: Votiva (DEVICE).
Who is sponsoring clinical trial NCT03536819?
This trial is sponsored by InMode MD, which has 22 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03536819's enrollment target sits among peer trials
20 1768th of 2000 higher than 140 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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