BTL Emsella Chair for Overactive Bladder
This study is testing the BTL Emsella Chair, a device that uses electromagnetic technology, to see if it can help people with overactive bladder (OAB). OAB causes symptoms like needing to urinate often or urgently. The Emsella Chair works by causing deep pelvic floor muscle contractions, similar to many Kegel exercises. Researchers want to compare its effectiveness against a "sham" Emsella Chair, which provides some sensation but no active treatment. The study aims to enroll 166 participants, including both men and women aged 18 and older who have had bladder symptoms for at least three months. Success will be measured by how many participants report their bladder symptoms are "moderately improved" or "markedly improved" after treatment. The study's current status is unclear.
- Study design
- This interventional study plans to enroll 166 participants. It compares the BTL Emsella Chair to a sham device.
- What's involved
- You would receive two treatments per week for a total of four weeks. You would also complete study questionnaires and communicate with staff about any side effects.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your bladder symptoms will be evaluated four weeks after completing all treatments, which is at week 8 of the study.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
BTL Emsella Chair Versus Sham for the Treatment of Overactive Bladder
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Kenneth Peters, MD · PRINCIPAL_INVESTIGATOR · Corewell Health William Beaumont University Hospital
Who to contact
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Do you actually qualify for this trial?
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Exclusion
What this trial measures
- Compare the efficacy of Emsella Chair versus Sham by evaluating the proportion of subjects reporting "moderately improved" or "markedly improved" responses on the Global Response Assessment (GRA) for overall bladder symptoms.4 weeks after completing all treatments; week 8 of the study
The GRA evaluates the patients' perceptions of overall improvement in symptoms on a 7-point scale (markedly worse, moderately worse, mildly worse, unchanged, slightly improved, moderately improved, markedly improved).