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NCT04133675 · ClinicalTrials.gov registry record · NA

BTL Emsella Chair Versus Sham for the Treatment of Stress Urinary Incontinence

A NA study of Stress Urinary Incontinence, sponsored by Corewell Health East.

Recruiting
Registry status
NA
Development phase
110
Enrollment target
1
Study location

NCT04133675 is a NA study of Stress Urinary Incontinence that is actively recruiting participants, run by Corewell Health East. The registered enrollment target is 110 participants, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (31% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04133675, a NA study of Stress Urinary Incontinence, is actively recruiting participants, sponsored by Corewell Health East.

RECRUITING
Registry status
NA
Development phase
110 participants
Enrollment target
1
Study location

Study Summary

Stress urinary incontinence (SUI) is a condition that affects both men and women. SUI is the involuntary leakage of urine caused by an increase in intra-abdominal pressure from activities such as exercise, coughing, laughing, or sneezing. It can significantly affect quality of life as patients avoid activities or behaviors that cause leakage. This clinical trial will compare the efficacy of the Emsella chair to sham and determine if electromagnetic technology is effective in the treatment of SUI.

Interventions

  • DEVICE BTL Emsella
  • DEVICE Sham BTL Emsella

Study Locations (1)

Michigan

  • Corewell Health William Beaumont University Hospital - Royal Oak

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2019-12-18
Est. Completion 2028-12
Phase NA

Sponsor

Corewell Health East

106 total trials

What the Registry Record Tells You About NCT04133675

The ClinicalTrials.gov registry entry for NCT04133675 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (31% lower). The listed sponsor is Corewell Health East, which has 106 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Stress Urinary Incontinence appearing as the primary indexed condition, and to 2 interventions - of which BTL Emsella is the first listed.

NCT04133675 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT04133675 about?

NCT04133675 is a clinical study titled "BTL Emsella Chair Versus Sham for the Treatment of Stress Urinary Incontinence". Stress urinary incontinence (SUI) is a condition that affects both men and women. SUI is the involuntary leakage of urine caused by an increase in intra-abdominal pressure from activities such as exercise, coughing, laughing, or sneezing. It can significantly affect quality of life as patients avoid...

What is the current status of trial NCT04133675?

This trial is currently recruiting. It is a NA study. The enrollment target is 110 participants. The study started on 2019-12-18. Estimated completion is 2028-12.

What conditions does trial NCT04133675 study?

This clinical trial studies the following conditions: Stress Urinary Incontinence.

What interventions are being tested in trial NCT04133675?

The interventions under investigation include: BTL Emsella (DEVICE), Sham BTL Emsella (DEVICE).

Who is sponsoring clinical trial NCT04133675?

This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04133675 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.