Diluted Aqueous Povidone-Iodine Compared to Saline to Decrease Surgical Site Infections
- Disease/Condition
- Surgical Site Infection
- Drug/Device/Intervention
- Povidone-Iodine
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Loma Linda University
- Location
- Loma Linda, United States of America
- Phase
- Phase 3
- Start date
- May 01, 2024
- End date
- Nov 01, 2025
- Enrollment
- 1100 participants
Surgical Site Infection
This is a multicenter randomized controlled trial of 1100 patients to evaluate the
 superiority of combined intraoperative wound irrigation with intraoperative peritoneal lavage
 with dilute aqueous povidone-iodine compared to normal saline in male and female patients
 between the ages of 18 and 80 years old undergoing emergency laparotomies with Centers for
 Disease Control (CDC) class 2 and 3 wounds.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06363877
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06363877 through Pure Global AI's free database. This Phase 3 trial is sponsored by Loma Linda University and is currently Not yet recruiting. The study focuses on Surgical Site Infection. Target enrollment is 1100 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.