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Starting soon Observational

Incidence of Ssi After c.s

NCT07476261 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2026-05-01
Last updated
2026-03-17

Condition(s) studied

Site Infection

Study summary

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

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * All women who underwent cesarean section during the study period Exclusion Criteria: * Patients who are lost to follow-up before completion of the 30-day postoperative assessment. Patients with immunocompromised conditions, such as: Chronic corticosteroid therapy. Immunosuppressive treatment. Known HIV infection with severe immunosuppression .

Primary outcome measure(s)

  • incidence of surgical site infection after cesarean section — Baseline
    superficial or deep surgical site infection

Trial sites (1)

FacilityCityRegionStatus
El Mabarra Health Insurance Hospital. Asyut Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07476261 on ClinicalTrials.gov ↗ ← All trials in Egypt