Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
NCT06975033

Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP

Led by University of California, San Francisco · Updated on 2026-04-16

114

Participants Needed

3

Research Sites

56 weeks

Total Duration

On this page

Sponsors

U

University of California, San Francisco

Lead Sponsor

S

State University of New York - Upstate Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This will be a randomized interventional study. Patients scheduled to undergo a HoLEP at UCSF will be randomized into two groups after the procedure: one group will watch a scripted educational HoLEP video and the other group will not receive a video. We will monitor the post-operative care utilization after discharge. Secondary outcomes will include patient satisfaction.

CONDITIONS

Official Title

Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 or older
  • Patients scheduled for a HoLEP procedure
  • Patients willing to complete both baseline and follow-up surveys
  • Patients able to provide informed consent
  • Patients who speak and understand English
Not Eligible

You will not qualify if you...

  • Patients under 18 years old
  • Patients unable to provide consent
  • Patients unable to complete surveys
  • Patients without a prostate
  • Patients who do not speak English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

University of California, San Francisco

San Francisco, California, United States, 94143

Actively Recruiting

2

University of Rochester Medical Center

Rochester, New York, United States, 14620

Not Yet Recruiting

3

Scott SUNY Upstate Medical University

Syracuse, New York, United States, 13210

Not Yet Recruiting

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Research Team

D

David Bayne, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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