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HoLEP Sexual Survivorship

NCT07660068 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 252

Last updated 2026-06-22

No results posted yet for this study

Summary

The objective of this study is to evaluate how sexual function, ejaculatory function, and overall sexual satisfaction change following Holmium Laser Enucleation of the Prostate (HoLEP).

In doing so, the study team will examine the trade-off between relief of lower urinary tract symptoms and changes in sexual function.

Conditions

  • BPH
  • Lower Urinary Tract Symptoms

Interventions

OTHER

Telephone Interview

A one-time 30-45-minute telephone interview and discussion regarding the participants' after HoLEP experience and sexual satisfaction following HoLEP.

OTHER

Questionnaires over the span of 24 months

Participants will complete questionnaires at 1, 3, 6, 12, and 24 months post-operatively

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-30
Primary Completion
2027-06-30
Completion
2029-06-30

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 NCT07660068 on ClinicalTrials.gov