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Single Dose Cefepime Versus Cefuroxime Plus Metronidazole as a Prophylactic Antibiotic During Emergency Intrapartum Cesarean Section

A

Assiut University

Status and phase

Unknown
Phase 3
Phase 2

Conditions

Infection Wound
Emergency Cesarean Section

Treatments

Drug: Cefuroxime plus Metronidazole
Drug: Cefepime

Study type

Interventional

Funder types

Other

Identifiers

NCT04009772
Antibiotic CS

Details and patient eligibility

About

Compare between cefepime versus routine antibiotics as a prophylactic antibiotic during emergency cesarean section in a tertiary center of obstetric care

Full description

This is a randomized double blinded study which compare between single dose cefepime versus cefuroxime plus metronidazole during emergency intrapartum cesarean section.

Outcomes will include fever, wound infection, and urinary tract infection.

Enrollment

500 estimated patients

Sex

Female

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • intrapartum caesarean section

Exclusion criteria

  • evidence of infection

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

500 participants in 2 patient groups

"Cefepime" , "Maxipime®" 1 gm
Active Comparator group
Description:
Patient will receive "Cefepime" ,"Maxipime®" 1 gm IV during cesarean section just before skin incision
Treatment:
Drug: Cefepime
"Cefuroxime", "Zinnat®" 1gm plus "metronidazole"Flagyl®" 500
Active Comparator group
Description:
Patient will receive "Cefuroxime", "Zinnat®" 1gm ,and "metronidazole"Flagyl®" 500 IV; just before skin incision for emergency cesarean section
Treatment:
Drug: Cefuroxime plus Metronidazole

Trial contacts and locations

1

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Central trial contact

Osama Abdalmageed; Abdalmageed Abdalmageed

Data sourced from clinicaltrials.gov

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