HoLEPNCT06975033
Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP
A study testing Video in people with HoLEP and Patient Satisfaction, run by University of California, San Francisco at 3 sites in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older, men only
- Conditions the study is for
- HoLEP, Patient Satisfaction, Educational Video Intervention
- What is being tested?
- Video
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 114 participants
- Where
- 3 sitesUnited States
- Study dates
- 4 Nov 2025to 1 Dec 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Men only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Adults aged 18+
- Patients scheduled for a HoLEP procedure
- Patients willing to complete both baseline and follow up surveys
- Patients able to provide informed consent
- Patients are English-speaking and understand English
Who cannot join
- Patients under 18+
- Patients unable to consent
- Patients unable to complete surveys
- Patients without a prostate.
- Patients are non-English speakers
Trial locations and contacts
3 sites in 1 country. Contact the study team or a site near you to ask about taking part.
United States3 sites, 3 recruiting
- Not yet recruiting
University of Rochester Medical Center
Rochester, New York, 14620
Scott Quarrier Quarier, scott_quarrier@urmc.rochester.edu
Rajat Jain, rajat_jain@urmc.rochester.edu
- Recruiting
University of California, San Francisco
San Francisco, California, 94143
David Bayne Bayne, 617-571-5870, david.bayne@ucsf.edu
- Not yet recruiting
Scott SUNY Upstate Medical University
Syracuse, New York, 13210
Scott Wiener Wiener, 774-239-2512, wienersc@upstate.edu
About this study
Official title: The Impact of Discharge Educational Discharge Videos on Post-Operative Care Utilization After Holmium Laser Enucleation of the Prostate (HoLEP) Procedures
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
- Being tested
- Video
- Medical subject headings
- Patient Satisfaction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
VideoOther
Participants will watch video.
| Study group | Role | What they receive |
|---|---|---|
| Video | Experimental | Participants will watch video. Receives: Other: Video |
| No Video | No intervention | Participants will not watch video. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Post-operative Healthcare Utilization Events
Healthcare utilization will include MyChart messages, phone calls to clinic, unscheduled clinic visits, hospital readmissions, and emergency/urgent care visits.
Measured: up to 90 days (estimated time frame between initial surgery and first follow up visit)
Participant Satisfaction Score
Measured using Likert scale survey ranging from 1 (strongly agree) to 5 (strongly disagree).
Measured: up to 90 days (estimated time frame between initial surgery and first follow up visit)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 May 2025
- Study start4 Nov 2025
- Primary completion1 Dec 2026 (estimated)
- Study completion1 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HoLEPStudies of the same condition, open and under way.
- More trials run by University of California, San FranciscoThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 114 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of California, San Francisco
- Sponsor type
- University, hospital or other
- Collaborators
- State University of New York - Upstate Medical University, University of Rochester
- Responsible party
- Sponsor
- Investigators
- David Bayne, MD, MPH, Principal investigator, University of California, San Francisco
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06975033
- Sponsor's protocol ID
- 25-43311
- Status last verified
- Apr 2026
- First submitted
- 4 Apr 2025
- Last updated
- 16 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Impact of Discharge Educational Discharge Videos on Post-Operative Care Utilization After Holmium Laser Enucleation of the Prostate (HoLEP) Procedures
- ClinicalTrials.gov ID
- NCT06975033
- Acronym / sponsor ID
- 25-43311
- Conditions
- HoLEP, Patient Satisfaction, Educational Video Intervention
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 114 participants (estimated)
- Lead sponsor
- University of California, San FranciscoUniversity, hospital or other
- Collaborators
- State University of New York - Upstate Medical University, University of Rochester
- Study start
- 4 Nov 2025 (actual)
- Primary completion
- 1 Dec 2026 (estimated)
- Study completion
- 1 Dec 2026 (estimated)
- First posted
- 16 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Video | Experimental | Other: VideoParticipants will watch video. |
| No Video | No intervention | –Participants will not watch video. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Adults aged 18+
- Patients scheduled for a HoLEP procedure
- Patients willing to complete both baseline and follow up surveys
- Patients able to provide informed consent
- Patients are English-speaking and understand English
Key exclusion criteria (5 listed)
- Patients under 18+
- Patients unable to consent
- Patients unable to complete surveys
- Patients without a prostate.
- Patients are non-English speakers
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| VideoParticipants will watch video. | Other | Video |
Primary outcome
Number of Post-operative Healthcare Utilization Events
Time frame: up to 90 days (estimated time frame between initial surgery and first follow up visit)
Healthcare utilization will include MyChart messages, phone calls to clinic, unscheduled clinic visits, hospital readmissions, and emergency/urgent care visits.
Participant Satisfaction Score
Time frame: up to 90 days (estimated time frame between initial surgery and first follow up visit)
Measured using Likert scale survey ranging from 1 (strongly agree) to 5 (strongly disagree).
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Apr 2026.
- Individual participant dataSharing planned: No
Related trials for HoLEP
Active, not recruitingPhase 2/3
Examining the Effects of Intra-detrusor Botox at Time of HoLEP in Men With Overactive Bladder Symptoms
Urinary Incontinence, Overactive Bladder Syndrome
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Learning Curve of Tri-lobar HoLEP Versus En-bloc HoLEP
Benign Prostatic Hyperplasia With Outflow Obstruction
RecruitingObservational study
Impact of Long-term Dutasteride Use on Perioperative Outcomes of HoLEP
Prostatic Hyperplasia, Benign
Not yet recruiting
Anterior Bridge-Preserving Versus Conventional Early Apical Release During Holmium Laser Enucleation of the Prostate
Benign Prostatic Hyperplasia, Benign Prostatic Obstruction
Not yet recruiting
Orientation Video Training Administered at Different Times to Patients Undergoing Prostate Surgery on Postoperative Pain and Anxiety (Video Training)
Benign Prostate Hypertrophy(BPH)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
David Bayne, MD, MPH principal investigator
University of California, San Francisco
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Video in people with HoLEP and Patient Satisfaction, run by University of California, San Francisco at 3 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 16 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact David Bayne, MD, MPH (617-571-5870, david.bayne@ucsf.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of Post-operative Healthcare Utilization Events (time frame: up to 90 days (estimated time frame between initial surgery and first follow up visit)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Apr 2026.