Status:

COMPLETED

The Skin Prep Study

Lead Sponsor:

Washington University School of Medicine

Conditions:

Surgical Site Infections

Eligibility:

FEMALE

Phase:

NA

Brief Summary

The investigators propose a randomized controlled clinical trial to determine the comparative effectiveness of chlorhexidine-alcohol and iodine-alcohol preoperative skin preparation for preventing sur...

Detailed Description

RESEARCH DESIGN AND METHODS This will be a randomized controlled clinical trial aimed at determining the comparative effectiveness of chlorhexidine-alcohol and iodine-alcohol preoperative skin prepar...

Eligibility Criteria

Inclusion

  • Women undergoing cesarean delivery at Barnes-Jewish Hospital.

Exclusion

  • Inability to obtain consent; allergy to chlorhexidine, alcohol, iodine, shellfish; and evidence of infection adjacent to operative site.

Key Trial Info

Start Date :

September 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2015

Estimated Enrollment :

1147 Patients enrolled

Trial Details

Trial ID

NCT01472549

Start Date

September 1 2011

End Date

June 1 2015

Last Update

August 8 2018

Active Locations (1)

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1

Barnes-Jewish Hospital

St Louis, Missouri, United States, 63108