Clinical Trial

Evaluation of Surgical Site Infection After Cesarean Section

Completed
View on ClinicalTrials.gov →
Summary
This study aims to investigate surgical site monitoring after cesarean section using a mobile application currently being developed. This mobile application aims to facilitate early diagnosis of surgical site infection, reduce clinic visits for wound monitoring, and consequently reduce labor, travel, and care costs. In this context, a randomized controlled design will be conducted between the study and control groups to compare surgical site infection rates, time to diagnosis, number of clinic visits, frequency of hospitalization, care costs, and patient satisfaction.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-09-25.
Status change: Enrolling by Invitation → Completed 2026-02-28
Trial Details
NCT Number NCT07205939
Lead Sponsor Sibel Bulut Haklı
Conditions Surgical Infection, Cesarean Section Wound
Enrollment 216 participants
Start Date 2025-01-05
Primary Completion 2026-01-20 (estimated)
Study Completion 2026-02-05 (estimated)
Updated on ClinicalTrials.gov 2026-03-03