Status:
COMPLETED
Evaluation of Wound Infection Rates and Cosmetic Results of Different Suture Materials in Cesarean Skin Incision
Lead Sponsor:
Ayşenur Çalış Özbayram
Conditions:
Cesarean Section; Infection
Scar
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
Our primary aim is to determine the most beneficial suture in order to reduce complications due to skin incision in common surgeries such as cesarean section, and our secondary aim is to evaluate the ...
Detailed Description
Patients who met the inclusion criteria among patients who had a cesarean delivery (January 2023-June 2023) in our hospital within a 6-month period will be included in the study. Patients included in ...
Eligibility Criteria
Inclusion
- 18-45 years old
- Patients who had a primary cesarean section at our \>37w hospital
- Patients with a Pfannenstiel incision closed subcutaneously
Exclusion
- Women \<18 years and \>45 years old
- Those with a history of keloid
- Suprapubic incision due to previous surgery
- Signs of infection at or near the incision during cesarean section
- Known hypersensitivity to any of the suture materials used
- Having a medical condition that causes immunosuppression, such as DM, chronic corticosteroid use
- Failure to obtain informed consent from the patient
Key Trial Info
Start Date :
February 22 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 22 2023
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT06119113
Start Date
February 22 2023
End Date
October 22 2023
Last Update
December 18 2025
Active Locations (1)
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1
Başakşehir Çam Ve Sakura Şehir Hastanesi
Istanbul, Başakşehir, Turkey (Türkiye), 00034