Cosmetic results after different methods of subcutaneous tissue and skin closure in cesarean section in obese women: a randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201909687336867

Enrollment

180

Registered

2019-09-25

Start date

2019-08-01

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy and Childbirth

Interventions

prolene group

vicryl group

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Patients age 18-45 years, Patients with previous CS, Patients' BMI = 30 kg/m2.

Exclusion criteria

Exclusion criteria: a) Clinical signs of chorioamnionitis at the time of CS, b) HELLP syndrome or preeclampsia, c) History of keloid scar formation, d) Medical disorders that could affect wound healing( known hypersensitivity to any of the suture materials used in the study, diabetes mellitus, chronic corticosteroid use or immunosuppression) e) Emergency CS, f) History of ruptured membranes before CS and g) Patients refusing to participate in the study.

Design outcomes

Primary

Measure	Time frame
effect pf different closure methods on the appearance of the scare 6 months after cs	—

Secondary

Measure	Time frame
complications related to the scare	—

Countries

Egypt

Contacts

Public Contactomima taha

suez canal university

omimatharwat@yahoo.com01223423685

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026