Status:
NOT_YET_RECRUITING
Comparative Analysis of Subcuticular Suture Materials in Cesarean Section
Lead Sponsor:
Cairo University
Collaborating Sponsors:
Kafrelsheikh University
Conditions:
Cesarean Wound Disruption With Postnatal Complication
Eligibility:
FEMALE
20-45 years
Phase:
NA
Brief Summary
1.1. Background and Rationale Cesarean section is one of the most common surgical procedures performed worldwide. The choice of suture material for closing the skin incision is crucial, as it can infl...
Detailed Description
2.1. Surgical Techniques in Cesarean Section Cesarean section involves multiple surgical steps, including skin incision, uterine incision, and closure of the incisions. The subcuticular suturing techn...
Eligibility Criteria
Inclusion
- Women aged 20-45 years old.
- BMI = or more than 40 kg/m2
- Primigravida or not more than the previous 1 cesarean section.
- Will undergo a lower-segment cesarean section.
- Hb: ≥ 10 gm/dl.
- Viable fetus.
- No history of medical comorbidities.
Exclusion
- History of urogenital tract infection within 2 weeks before cesarean delivery.
- Presence of clinical signs of infection at the time of delivery including PPROM and intraamniotic infection.
- Medical comorbidities (hypertension, diabetes, etc.).
- Hypersensitivity to any of the suture materials.
- Women with abnormal placentation (placental abruption or placenta previa).
- History of systemic corticosteroid intake during their pregnancy for 2 weeks or more.
- History of previous surgical site infection.
- Immune-compromised women.
- Women refused to participate in the study or could not obtain consent.
Key Trial Info
Start Date :
August 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 30 2025
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT06543329
Start Date
August 1 2024
End Date
August 30 2025
Last Update
August 9 2024
Active Locations (1)
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1
faculty of medicine, Kasr el ainy hospital, Cairo university
Cairo, Egypt, 11562