Clinical Trials Directory

Trials / Completed

CompletedNCT01700803

Povidone Iodine and Cesarean Section Wound Infections

Povidone Iodine 10% Versus 7.5% Hand Scrub and Cesarean Section Wound Infections: A Randomized Trial

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
3,231 (actual)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The aim of this randomized clinical trial is to compare the efficiency of hand scrubbing by Povidone-Iodine solution 10% over 7.5% concentration in decreasing post-cesarean section wound infections \& compare side effects of both agents.

Detailed description

For centuries, hand washing with soap and water has been considered the main approach for personal hygiene. In the community, hand hygiene has been known to prevent infectious diseases and to decrease the burden of disease. Currently, hand hygiene is considered the most important measure for preventing the spread of pathogens in health-care settings. There are multiple agents used for surgical hand scrubbing as alcohol, chlorhexidine, iodine/iodophors, para-chloro-meta-xylenol \& triclosan. Ideally, the optimum antiseptic used for scrub should have broad spectrum of activity, persistent effect \& fast acting. Unfortunately most studies evaluating surgical scrub antiseptics have focused on measuring hand bacterial colony counts. No randomized clinical trials have evaluated the impact of surgical scrub choice on surgical site infection risk \& proven its efficiency.

Conditions

Interventions

TypeNameDescription
DRUGPovidone Iodine 10% vand cesarean section wound infections
DRUGPovidone Iodine 7.5% vand cesarean section wound infections

Timeline

Start date
2012-01-01
Primary completion
2012-04-01
Completion
2012-05-01
First posted
2012-10-04
Last updated
2012-10-04

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT01700803. Inclusion in this directory is not an endorsement.