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Prophylactic Ceftizoxime (Cefizox) for Elective Cesarean Delivery

U

University of Khartoum

Status and phase

Completed
Phase 4

Conditions

Caesarean

Treatments

Drug: ceftizoxime

Study type

Interventional

Funder types

Other

Identifiers

NCT01347593
ceftizoxime cesarean

Details and patient eligibility

About

Ceftizoxime (Cefizox) will reduce post Cesarean delivery febrile morbidity.

Enrollment

220 patients

Sex

Female

Ages

14 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective Cesarean section

Exclusion criteria

  • Diabetes severe anaemia allergy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

220 participants in 1 patient group

ceftizoxime (cefizox) injection
Experimental group
Description:
ceftizoxime (cefizox) as single dose of 1 g at the interval of 30-60 minutes before the incision
Treatment:
Drug: ceftizoxime

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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