Not Yet RecruitingNot Applicable

Incidence of Ssi After c.s

Egypt105 participantsStarted 2026-05-01

Plain-language 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.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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 .

What they're measuring

incidence of surgical site infection after cesarean section

Timeframe: Baseline

Trial details

NCT IDNCT07476261

SponsorAssiut University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-05-01

Contact for this trial

mona madgy

01145421696 mona.helmy1997@gmail.com

View on ClinicalTrials.gov More Site Infection trials