NCT05719220 Effect of Group Preoperative Pelvic Floor Training for HoLEP
| NCT ID | NCT05719220 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of California, San Francisco |
| Condition | BPH |
| Study Type | OBSERVATIONAL |
| Enrollment | 100 participants |
| Start Date | 2024-02-07 |
| Primary Completion | 2028-12-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 100 participants in total. It began in 2024-02-07 with a primary completion date of 2028-12-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The main goal of this study is to see if group pelvic floor training before surgery can help prevent urinary incontinence after Holmium laser enucleation of the prostate (HoLEP) surgery. The study has the potential to inform preoperative intervention strategies for managing incontinence after HoLEP.
Eligibility Criteria
Inclusion Criteria: * Consecutive patients with a diagnosis of BPH with a plan to undergo HoLEP. * Between the age of 50-90. * Ability to understand and provide informed consent. Exclusion Criteria: * Patients whom inability to carry out PFT protocol. * Patients unwilling or unable to complete follow up care. * Severe urinary incontinence due to a history of neurological diseases such as a cerebrovascular accident or spinal cord injuries. * Patients whom inability to read and understand the English language.
Contact & Investigator
Max Bowman, M.D.
PRINCIPAL INVESTIGATOR
University of California, San Francisco
Frequently Asked Questions
Who can join the NCT05719220 clinical trial?
This trial is open to male participants only, aged 50 Years or older, up to 90 Years, studying BPH. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05719220 currently recruiting?
Yes, NCT05719220 is actively recruiting participants. Contact the research team at victoria.hogue@ucsf.edu for enrollment information.
Where is the NCT05719220 trial being conducted?
This trial is being conducted at San Francisco, United States.
Who is sponsoring the NCT05719220 clinical trial?
NCT05719220 is sponsored by University of California, San Francisco. The principal investigator is Max Bowman, M.D. at University of California, San Francisco. The trial plans to enroll 100 participants.