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Chlorhexidine vs. Iodine for Vaginal Preparation in Urogynecologic Procedures — CLNUP  

Urinary Incontinence Clinical Trial

Official title:
Chlorhexidine Gluconate Versus Povidone Iodine for Vaginal Surgical Preparation for Urogynecological Procedures

Clinical Trial Summary

This is a randomized controlled trial to determine if there is a difference between chlorhexidine gluconate and povidone iodine vaginal preparations for urogynecological surgery post operative infections.

Clinical Trial Description

The purpose of this randomized controlled trial is to determine whether there is a difference in efficacy of two of the most common commercially available vaginal surgical preparations. The first objective is to determine whether chlorhexidine gluconate is non-inferior to povidone iodine with respect to post-operative infections including urinary tract infections (both culture proven and empirically treated) and surgical site infections (as defined by the Centers for Disease Control). The second objective is to determine whether chlorhexidine gluconate is non-inferior to povidone iodine with respect to vulvar and vaginal irritation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04048356
Study type Interventional
Source University of New Mexico
Contact
Status Completed
Phase Phase 3
Start date July 15, 2019
Completion date March 14, 2021
View Details
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