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
| Type | Name | Description |
|---|---|---|
| DRUG | Cefepime 1000 MG | Cefepime is a fourth-generation cephalosporin antibiotic |
| DRUG | Ampicillin-sulbactam | Broad-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.