Clinical Trial

Enucleation Ratio as a Novel Predictor of Symptomatic Improvement After HoLEP

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Summary
The goal of this observational study is to determine whether the rate of prostate tissue removed during surgery relative to the preoperative total prostate volume (referred to as the "enucleation ratio") predicts symptomatic improvement 3 months after HoLEP. The main question it aims to answer is: \- What is the minimum enucleation ratio required to achieve clinically important symptomatic improvement? (Symptomatic improvement is referred to as a threshold of having an International Prostate Symptom Score (IPSS) lower than 8 points, which is determined by the American Urological Association (AUA) and European Association of Urology(EAU)).
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-05-09.
Trial Details
NCT Number NCT07591688
Lead Sponsor Ondokuz Mayıs University
Conditions Benign Prostate Obstruction (BPO)
Enrollment 400 participants
Start Date 2026-07-01
Primary Completion 2027-02-01 (estimated)
Study Completion 2027-03-30 (estimated)
Updated on ClinicalTrials.gov 2026-05-19