Incontinence Analysis After HoLEP Using 28Fr Versus 22Fr Sheath

Status Active, not recruiting

Clinical Trial Summary

The rationale for this study is to assess whether there is a difference in HoLEP outcomes in smaller 22Fr instruments compared to our standard 28Fr sheaths.

Clinical Trial Description

This study will be a randomized controlled trial in which patients who meet inclusion criteria will be randomized to one of two groups, HoLEP performed with either 1) 22Fr sheath set or 2) 28Fr sheath set. After HoLEP, data will be analyzed using chi-square test for incontinence vs no incontinence between 22Fr and 28Fr groups at 1 week, 4 weeks and 12 weeks post operatively. ;

Study Design

Related Conditions & MeSH terms

Urinary Incontinence

Clinical Trial Details

NCT number	NCT06068790
Study type	Interventional
Source	Indiana University
Contact
Status	Active, not recruiting
Phase	N/A
Start date	August 1, 2023
Completion date	July 1, 2025

View Details

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