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RECRUITING
NCT06691750
NA

Clinical Impact of Uterine Repair During Cesarean Section with Barbed Suture on the Incidence of Isthmocele

Sponsor: Hospital Clinic of Barcelona

View on ClinicalTrials.gov

Summary

Pregnant women, irrespective of their pregnancy risk, who undergo a cesarean section for any reason will be randomized to one of two suturing techniques: conventional suture or barbed suture for uterine repair after the cesarean section. Following surgery, these patients will be followed up for clinical outcomes, ultrasound evaluation of the uterine scar, and study of the hypoxic-inflammatory environment of the uterine cavity.

Official title: Clinical Impact of Uterine Repair During Cesarean Section with Barbed Suture on the Incidence of Isthmocele and Its Ultrasound and Molecular Characteristics: a Randomized Controlled Trial

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

364

Start Date

2024-11-22

Completion Date

2028-05

Last Updated

2025-03-13

Healthy Volunteers

Yes

Interventions

DEVICE

Barbed suture

Size 0 barbed absorbable monofilament suture with unidirectional spikes that includes a loop in one of its ends, not requiring knots.

DEVICE

Conventional smooth suture

Size 1 smooth multifilament absorbable polyglactin suture.

Locations (1)

Hospital Clínic de Barcelona

Barcelona, Spain