Incidence of Ssi After c.s
ConditionSite Infection
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorAssiut University
About this trial
aim of the work is to evaluate adherence to preoperative , intraoperative, and postoperative infection preventive measures during cesarean section and to assess it s impact on the incidence of surgical site infection and maternal well-being during 30 days postoperative peroid.
Eligibility criteria
Qualifiers
All women who underwent cesarean section during the study period
Disqualifiers
Patients who are lost to follow-up before completion of the 30-day postoperative assessment.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov