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Clinical Trial Summary

the aim of this study is to evaluate the efficacy of employing cefepime (CFM) versus ampicillin/sulbactam (AMS) in lowering the rate of post-cesarean surgical site infections.


Clinical Trial Description

A prospective randomized clinical study conducted in the department of obstetrics and gynecology of Beni-Suef University Hospital . A total of 213 women were assessed for eligibility, 13 of which were excluded. A total of 200 pregnant women who were eligible for elective cesarean sections (CS). The overall median duration of postoperative followed up was from 10 days to one month to determine the surgical site infection (SSI). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06048692
Study type Interventional
Source Beni-Suef University
Contact
Status Active, not recruiting
Phase Phase 3
Start date January 1, 2023
Completion date September 20, 2023

See also
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