Effect of prophylaxis antibiotic before and during operation on maternal and neonatal outcomes

Phase 3

Recruiting

• Conditions: Elective cesarean section.; Delivery by elective caesarean section

• Registration Number: IRCT20180525039834N1
• Lead Sponsor: Shahroud University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 July 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 360

Inclusion Criteria

Gestational age greater than 34 weeks

Exclusion Criteria

Antibiotic use in the past two weeks
The temperature greater than 38 at least 2 times at intervals of 6 hours in the axillary region during surgery
Sensitivity to cefazolin antibiotics

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Endometritis. Timepoint: Before surgery and 1 week and 2 weeks after surgery. Method of measurement: Clinical evaluation.;Wound infection. Timepoint: Before surgery and 1 week and 2 weeks after surgery. Method of measurement: Clinical evaluation.;Urinary tract infection. Timepoint: Before surgery and 1 week and 2 weeks after surgery. Method of measurement: Clinical evaluation.;Apgar Score. Timepoint: At birth. Method of measurement: Clinical evaluation.;Hypothermia. Timepoint: At birth. Method of measurement: Clinical evaluation.;Tachypnea. Timepoint: At birth. Method of measurement: Clinical evaluation.