Clinical Trials in Egypt / NCT07476261
Starting soon
Observational
Incidence of Ssi After c.s
NCT07476261 · tracked via the Priya Life Science Egypt tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| El Mabarra Health Insurance Hospital. | Asyut | Egypt |
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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