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NCT05287490 · ClinicalTrials.gov registry record · NA

Bi-Polar Radio-Frequency and Electrical Muscle Stimulation for Symptoms of Mixed Urinary Incontinence (MUI)

A NA study, sponsored by InMode MD.

Completed
Registry status
NA
Development phase
31
Enrollment target

NCT05287490 is a NA study that has completed, run by InMode MD. The registered enrollment target is 31 participants.

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The verdict

NCT05287490, a NA study, has completed, sponsored by InMode MD.

COMPLETED
Registry status
NA
Development phase
31 participants
Enrollment target

Study Summary

The objective of this trial is to evaluate the safety and efficacy of the combined FormaV and VTone Applicators for Symptoms of Mixed Urinary Incontinence. Eligible subjects will receive 3 treatments(every 2 weeks) with the FormaV and VTone Applicators according to the study protocol. The subject will return for 3 follow-up visits: 4 weeks (1M FU), 3 months follow up (3M FU), 6 months follow up (6M FU) after the treatment.

Interventions

  • DEVICE FormaV and VTone

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2021-04-04
Est. Completion 2022-07-30
Phase NA

Sponsor

InMode MD

22 total trials

What the Registry Record Tells You About NCT05287490

The ClinicalTrials.gov registry entry for NCT05287490 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is InMode MD, which has 22 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which FormaV and VTone is the first listed.

NCT05287490 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05287490 about?

NCT05287490 is a clinical study titled "Bi-Polar Radio-Frequency and Electrical Muscle Stimulation for Symptoms of Mixed Urinary Incontinence (MUI)". The objective of this trial is to evaluate the safety and efficacy of the combined FormaV and VTone Applicators for Symptoms of Mixed Urinary Incontinence. Eligible subjects will receive 3 treatments(every 2 weeks) with the FormaV and VTone Applicators according to the study protocol. The subject ...

What is the current status of trial NCT05287490?

This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2021-04-04. Estimated completion is 2022-07-30.

What interventions are being tested in trial NCT05287490?

The interventions under investigation include: FormaV and VTone (DEVICE).

Who is sponsoring clinical trial NCT05287490?

This trial is sponsored by InMode MD, which has 22 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.