Study details
Enrolling now
TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence
University of Rochester
NCT IDNCT06369922ClinicalTrials.gov data as of Apr 2026
Target enrollment
100
Study length
about 1.9 years
Ages
18+
Sex
Female only
Locations
1 site in NY
What this study is about
Researchers are testing whether using TENS during outpatient urethral bulking procedures helps manage pain. Women undergoing this procedure will be randomly assigned to either receive real TENS or a placebo TENS. The trial will last about 700 days.
Simplified from trial records by PatientMatch.
What you may be asked to do
- 1.Undergo Control TENS
- 2.Undergo TENS
Participation Burden
What's physically and logistically required of participants.
Logistics & Travel
In-person visits
Requires travel to a study site
Physical Intervention
Standard
How treatment is administered
Treatment Assignment
Randomized & Blinded
You may get a placebo/standard care, and you won't know which.
Extracted study details
Pulled from the trial record to show what is being tested and what the study is measuring.
Endpoints
Primary: Mean pain measured by Visual Analog Scale (VAS)
Secondary: Mean pain measured by Likert scale
Devices
therapeutic