gestation
Conditions
Interventions
intervention group:cefathiamidine was administered by the 30 minutes
control group:cefathiamidine was administered at cord clamping
Sponsors
Department of Pharmacy West China Second University Hospital, Sichuan University
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Subjects were eligible for the trial if they were older than 37 weeks estimated gestational; age and required cesarean delivery.
Exclusion criteria
Exclusion criteria: Exclusion criteria included cefathiamidine allergy, exposure to any antibiotic agent within 1 week of delivery, the temperature more than 37.5 degree C before cesarean or reject to participate in the trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endomyometritis;Wound infection;urinary tract infection;Neonatal sepsis;Neonatal sepsis workup;Neonatal admission;Neonatal dysbacteriosi; | — |
Secondary
| Measure | Time frame |
|---|---|
| Temperature after cesarean;Number of white blood count and neutrophile granulocyte after cesarean;ratio of neonatal stool coccus and bacillus; | — |
Countries
China
Contacts
Public ContactZhang Lingli
Outcome results
None listed