Expired Study
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Saint Louis, Missouri 63110


Purpose:

The purpose of this study is to evaluate cefoxitin pharmacokinetics in obese surgical patients.


Criteria:

Inclusion Criteria: - BMI <25 and >40 - Scheduled for elective abdominal or pelvic surgery - Surgical plan for intraoperative cefoxitin prophylaxis - Able to provide informed consent Exclusion Criteria: - Allergy to Cefoxitin - Renal or Hepatic insufficiency


NCT ID:

NCT00752908


Primary Contact:

Principal Investigator
Evan D Kharasch, MD, PhD
Washington University School of Medicine


Backup Contact:

N/A


Location Contact:

Saint Louis, Missouri 63110
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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