MedTrace Logo

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

NCT06975033 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2026-04-16

No results posted yet for this study

Summary

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

  • HoLEP
  • Patient Satisfaction
  • Educational Video Intervention

Interventions

OTHER

Video

Participants will watch video.

Sponsors & Collaborators

Principal Investigators

  • David Bayne, MD, MPH · University of California, San Francisco

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-04
Primary Completion
2026-12-01
Completion
2026-12-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06975033 on ClinicalTrials.gov