Status:
ENROLLING_BY_INVITATION
Evaluation of Surgical Site Infection After Cesarean Section
Lead Sponsor:
Sibel Bulut Haklı
Conditions:
Surgical Infection
Cesarean Section Wound
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief 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 surgi...
Detailed Description
While birth occurs spontaneously and naturally at the end of pregnancy due to a woman's normal physiology, intervention is required if a condition endangers the pregnant woman or the fetus. Cesarean s...
Eligibility Criteria
Inclusion
- Women who have had a Caesarean section Owning a smartphone with internet access Ages 18-45 Providing informed consent Adequate Turkish reading comprehension
Exclusion
- Presence of illnesses that prevent the use of the online survey/application (visual impairment, neuropsychiatric illnesses, etc.).
- Failure to comply with working conditions (not completing forms, missing forms, etc.)
- \-
Key Trial Info
Start Date :
January 5 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2026
Estimated Enrollment :
216 Patients enrolled
Trial Details
Trial ID
NCT07205939
Start Date
January 5 2025
End Date
March 1 2026
Last Update
October 3 2025
Active Locations (1)
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1
Istinye University
Istanbul, Turkey (Türkiye)