Incidence of Ssi After c.s

Starting soon

Conditions studied: Site Infection

In brief

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.

Key facts

Study ID

NCT07476261

Run by

Assiut University

People needed

105

Starts

2026-05-01

Expected to finish

2027-08-01

Last updated by the study team

2026-03-17

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• All women who underwent cesarean section during the study period

You may not qualify if…

• 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 .

Where it is running

• El Mabarra Health Insurance Hospital. — Asyut, Egypt

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.