Clinical Trials Directory

Trials / Unknown

UnknownNCT06048692

Cefepime and Unictam on Preventing Post-Cesarean Surgical Site Infections

The Impact of Cefepime and Unictam on Preventing Post-Cesarean Surgical Site Infections

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
213 (actual)
Sponsor
Beni-Suef University · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

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.

Detailed 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).

Conditions

Interventions

TypeNameDescription
DRUGCefepime 1000 MGCefepime is a fourth-generation cephalosporin antibiotic
DRUGAmpicillin-sulbactamBroad-Spectrum Antibiotic

Timeline

Start date
2023-01-01
Primary completion
2023-09-15
Completion
2023-09-20
First posted
2023-09-21
Last updated
2023-09-21

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06048692. Inclusion in this directory is not an endorsement.