Status:
RECRUITING
BTL Emsella Chair Versus Sham for the Treatment of Stress Urinary Incontinence
Lead Sponsor:
Corewell Health East
Conditions:
Stress Urinary Incontinence
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief 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 exer...
Detailed Description
This is a prospective, sham-controlled, observational study of subjects undergoing electromagnetic perineal stimulation for the treatment of SUI. Eligible subjects will be randomized to receive active...
Eligibility Criteria
Inclusion
- Able to read, understand, and provide written, dated, informed consent prior to screening, and be likely to comply with study protocol, including independently complete study questionnaires and communicate with study personnel about AEs and other clinically important information.
- Females and males, 18 to 80 years of age, inclusive, at screening
- Positive Cough or Bladder Stress Test at screening
- Subject agrees not to start any new treatment (medication or otherwise) during the treatment and follow-up periods.
- 6\. Subject agrees to maintain a stable dose of any medication known to affect lower urinary tract function, including but not limited to anticholinergics, tricyclic antidepressants, beta-3 adrenergic agonist, or α-adrenergic blockers, throughout the treatment and follow-up periods.
- For Females Only:
- Subject agrees to discontinue use of bladder support devices, including but not limited to vaginal pessary, during the screening, treatment, and follow-up periods.
- If of child-bearing age and female, agree to practice approved birth-control methods (oral contraceptives, condom barrier, injection, diaphragm or cervical cap, vaginal contraceptive ring, IUD, implantable contraceptive, surgical sterilization (bilateral tubal ligation), vasectomized partner(s))
- For Males Only:
- \- Subject must be ≥ 4 months post radical prostatectomy
Exclusion
- Pelvic floor physical therapy, including muscle training and/or electrostimulation, in a clinical setting within 30 days prior to screening
- Subject is morbidly obese (defined as body mass index 40 or greater)
- Pulmonary insufficiency, defined as difficulty breathing and fatigue, especially during exercise; chest pain, such as squeezing, pressure or tightness; the sensation of rapid or irregular heartbeat (palpitations); swelling of the legs or feet; dizziness or fainting; and/or bluish discoloration of the nails and/or lips (cyanosis)
- Any condition that causes a lack of normal skin sensation to the pelvis, buttocks, and lower extremities
- Implanted cardiac pacemaker or metal in the body, including, but not limited to drug pumps, neurostimulators, electronic implants, copper intrauterine devices (IUDs), and/or defibrillators
- Subject has a piercing between the waist and knees and is not willing to remove it before each treatment
- Active urethral diverticula
- Known vesicoureteral reflux
- Currently healing from surgical procedures where muscle contraction may disrupt the healing process
- Treatment with urethral bulking agents within the 6 months prior to the Screening Visit
- Subject is currently receiving treatment for a malignant tumor that would interfere with study participation.
- Subject has used the BTL EMSELLA device previously
- Subject has urinary incontinence of neurogenic etiology, such as multiple sclerosis, spina bifida, Parkinson's, spinal cord injury, diabetic neuropathy etc.
- Clinically confirmed urinary tract infection, requiring treatment as determined by the investigator, at the Screening Visit
- Currently participating in an investigational study that may impact study results or previously received an investigational drug or treatment within 30 days of the Screening Visit
- Current or history of any physical condition that, in the investigator's opinion, might put the subject at risk or interfere with study results interpretation
- For Females Only:
- Pregnant, or planning to become pregnant, at screening or anytime throughout the study period
- History of surgery with insertion of vaginal mesh for SUI
- Vaginal prolapse beyond the introitus
- Vaginal rejuvenation treatment, including laser treatments and radiofrequency therapy, within the 6 months prior to the Screening Visit
- Note for the sake of preserving scientific integrity, one or more of the eligibility criteria have been left off the list posted while the trial is ongoing. A full list of eligibility criteria will be posted upon completion of the trial.
Key Trial Info
Start Date :
December 18 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2028
Estimated Enrollment :
110 Patients enrolled
Trial Details
Trial ID
NCT04133675
Start Date
December 18 2019
End Date
December 1 2028
Last Update
December 11 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Corewell Health William Beaumont University Hospital
Royal Oak, Michigan, United States, 48073