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Cesarean Wound; Dehiscence clinical trials

View clinical trials related to Cesarean Wound; Dehiscence.

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NCT ID: NCT05166174 Completed - Clinical trials for Cesarean Section Complications

Lower Uterine Segment Following a Cesarean Section With Barbed Suture

BARB-LOWSEGM
Start date: January 1, 2019
Phase:
Study type: Observational

This aim of this study is to investigate the LUS in the pregnancy following a previous cesarean section with the use of barbed or conventional smooth suture.

NCT ID: NCT04371549 Completed - Clinical trials for Cesarean Wound; Dehiscence

Skin Closures at Cesarean Delivery, Glue vs Subcuticular Sutures.

Start date: August 25, 2020
Phase: N/A
Study type: Interventional

The optimal choice of skin closure at cesarean delivery has not yet been determined. This study will compare wound complications and scar healing following cesarean delivery between 2 methods of skin closure: glue (Dermabond®; Ethicon, Somerville, NJ) and monofilament (Monocryl®; Ethicon) epidermal sutures.

NCT ID: NCT04198324 Completed - Clinical trials for Cesarean Section; Dehiscence

Isthmocele After Endometrial and Non-endometrial Suturing in Cesarean Section

Start date: December 16, 2019
Phase: N/A
Study type: Interventional

This study compares the effect of two techniques of uterine closure, with or without endometrial suturing on isthmocele development after cesarean section.

NCT ID: NCT03609281 Completed - Clinical trials for Cesarean Section; Dehiscence

Cesarean Scar Characteristics After Scheduled and Emergency Cesarean Deliveries

Start date: August 1, 2018
Phase:
Study type: Observational [Patient Registry]

This study was designed to evaluate the scar characteristics following scheduled and emergency cesarean deliveries.

NCT ID: NCT03414762 Completed - Clinical trials for Cesarean Section Complications

PICO Negative Pressure Wound Therapy in Obese Women Undergoing Elective Cesarean Delivery.

Start date: April 1, 2019
Phase: Phase 3
Study type: Interventional

A randomized controlled, parallel group, superiority, open-label, single-institution, Phase 3 interventional clinical trial to evaluate clinical outcomes in obese gravidas undergoing elective cesarean delivery whose wounds were dressed with the PICO Negative Pressure Wound Therapy (NPWT) versus the standard dressing. We hypothesize that the PICO NPWT will reduce the incidence of surgical site occurrences and interventions and postoperative readmissions in obese women. The study will compare surgical site occurrences and surgical incision intervention incidence within 42 +/- 10 days post cesarean delivery in obese women who have the current standard-of-care dressing versus the PICO NPWT.