Efficacy Comparison of Two Preoperative Skin Antisepsis Preparations in Colorectal Surgery

Completed · Not applicable

Conditions studied: Colorectal Surgery

In brief

Surgical site infections (SSI) are one of the most common complications in the post-operative patient, and the second most common health care associated infection overall. It is estimated that there are between 500 thousand and 1.1 million surgical site infections in the United States each year. Given the magnitude of the problem, prevention of surgical site infections is a major goal of peri-operative care. However, skin preparation prior to surgery has not been as rigorously examined. The primary objective of this study is to compare the efficacy of two FDA approved, popular peri-operative skin preparations 2% chlorhexidine gluconate / 70% isopropyl alcohol to Iodine Povacrylex \[0.7% available Iodine\] / 74% Isopropyl Alcohol in the prevention of superficial surgical site infection. Male and female patients, age 18 years and older undergoing elective colorectal surgical procedures involving a laparotomy will be enrolled. These patients are at high risk of SSI. Eligible patients will be assessed at regular intervals for SSI and characterization of bacterial pathogen(s) in patients with SSI. Patients will remain enrolled into the study until 35 days postoperatively.

Key facts

Study ID

NCT01233050

Run by

University of Pennsylvania

People needed

802

Starts

2010-12-01

Expected to finish

2015-02-01

Last updated by the study team

2018-07-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18 years or older, male or female
• Undergoing any large bowel procedure with an extraction incision site(including ileostomy closure and Hartman's colostomy reversals).
• A clean-contaminated preoperative classification.
• Patient must have decision-making capacity and undergo appropriate informed consent process.
• Non-pregnant or post menopausal or surgically sterilized females. If of child-bearing age, patients must have a negative (serum or urine) pregnancy prior to surgery.

You may not qualify if…

• Antibiotics taken within 5 days prior to surgery.
• Infected wound classification.
• Preoperative evaluation that may preclude full closure of the skin.
• Undergoing any bowel procedure that will not result in an extraction incision.
• Ongoing radiation or chemotherapy treatment.
• Pregnant.
• Refusal to accept medically indicated blood products.
• Current abdominal wall infection or surgical site infection from previous laparotomy / laparoscopy.
• History of laparotomy within the last 60 days.
• Known allergy to iodine or to chlorhexidine gluconate.
• Participating in a preoperative antibiotic trial.
• Participating in a skin antisepsis trial.
• Participating in Ulcerative colitis trial conflicting with this trial.
• Women who are breast feeding (potential for transient hypothyroidism in the nursing newborn).

Where it is running

• Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania, United States
• Penn Presbyterian Medical Center — Philadelphia, Pennsylvania, United States
• Pennsylvania Hospital — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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