Sponsor:
UCLA
Code:
NCT07451106
Conditions
Postpartum Bladder Dysfunction
Post-prostatectomy Bladder Dysfunction
Bladder Dysfunction
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
DFree Non-Invasive Bladder Ultrasound
Perifit Kegel Exerciser
Exit interview
Brief summary:
Conditions
Postpartum Bladder Dysfunction
Post-prostatectomy Bladder Dysfunction
Bladder Dysfunction
Study ID
NCT07451106
Start date
Jul 11, 2024
Status verified date
Feb, 2026
Completion date
Jul, 2026
Anticipated
Primary completion date
Jul, 2026
Anticipated
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Enrollment
25 participants
Anticipated
Arms
Men post-prostatectomy with bladder dysfunction
Postpartum women with bladder dysfunction
Women with bladder dysfunction
Clinicians
Interventions
DFree Non-Invasive Bladder Ultrasound
Perifit Kegel Exerciser
Exit interview
Primary outcome measure
Central contacts
Locations
University of California San Francisco Weill Institute for Neurosciences
Recruiting
San Francisco, California, United States, 94158
Contacts
Principal Investigator:
Valerie Block, PT, DPTSc
Sponsor
University of California, San Francisco
Last update posted
Mar 5, 2026
Last verified
Feb, 2026
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of California, San Francisco on 2026-03-05.