Last updated: June 9, 2017
Sponsor: Poitiers University Hospital
Overall Status: Completed
Phase
4
Condition
N/ATreatment
N/AClinical Study ID
NCT02703857
PROPHYLOXITINE
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients who underwent major abdominal surgery whose forseeable time exceeds 4 hoursand requires an antibiotic prophylaxis by cefoxitin
Exclusion
Exclusion Criteria:
morbid obesity (BMI > 35 kg/m²)
severe renal impairment (clearance creatinine < 30ml/min)
beta lactam hypersensitivity
pregnancy
Study Design
Total Participants: 12
Study Start date:
February 01, 2016
Estimated Completion Date:
September 20, 2016
Connect with a study center
Centre Hospitalier de Poitiers
Poitiers, 86021
FranceSite Not Available

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