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Cesarean Section; Dehiscence clinical trials

View clinical trials related to Cesarean Section; Dehiscence.

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NCT ID: NCT06256822 Completed - Self Efficacy Clinical Trials

Technology-Based Breastfeeding Training After Cesarean

Start date: January 1, 2023
Phase:
Study type: Observational [Patient Registry]

Aim: The aim of this study was to determine the effect of breastfeeding training given with virtual reality (VR) to postpartum primiparous mothers on breastfeeding success and breastfeeding self-efficacy. Method: The research was designed as a prospective randomized controlled study. In total, 66 women were included in the study, with 31 in the control group and 35 in the intervention group. The intervention group watched a breastfeeding video with VR in the 4th and 24th hours after cesarean. Research data were collected with the sociodemographic information form, LATCH Breastfeeding Charting System and Documentation Tool and the Breastfeeding Self-Efficacy Scale. The study included mothers who gave birth with cesarean section, received breastfeeding counseling during pregnancy, with no vision or hearing disabilities and without any neurological disorder.

NCT ID: NCT05948150 Completed - Clinical trials for Cesarean Section; Dehiscence

The Effect of Breastfeeding Pillow on Breastfeeding Self-Efficacy and Postpartum Comfort in Women Who Had Cesarean

Start date: November 29, 2022
Phase: N/A
Study type: Interventional

The research is a randomised controlled experimental study. It was conducted to examine the effect of breastfeeding pillow on breastfeeding self-efficacy and postnatal comfort in primiparous puerperas who gave birth by caesarean section. The answers to the questions "Is the breastfeeding pillow effective on breastfeeding self-efficacy in primiparous puerperium giving birth by caesarean section?" and "Is the breastfeeding pillow effective on comfort during breastfeeding in primiparous puerperium giving birth by caesarean section?" are investigated. The puerperas in the experimental group were allowed to use a breastfeeding pillow during breastfeeding and evaluated at 24th and 48th hours. Puerperas in the control group continued routine breastfeeding and did not use a breastfeeding pillow. They were evaluated at 24th and 48th hours.

NCT ID: NCT05770115 Completed - Clinical trials for Cesarean Section; Dehiscence

A Randomized Clinical Study Based on Comparison Between Closure of Uterine Incision With Vicryl 2/0 Versus Vicryl 1 in Development of Uterine Niche.

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

The first group patients underwent double layer closure with split thickness with vicryl 2/0, in continuous, non- locked, 1 cm apart sutures, study group, and the second group, women underwent double layer closure with split thickness with vicryl 1, in continuous, non- locked, 1 cm apart sutures, control group. Then, all women in the study were followed up for development of niche within 1 to 6 weeks. The assessment after one week postpartum was with using trans-abdominal Ultrasound, then after two to six weeks postpartum with transvaginal Ultrasound

NCT ID: NCT05669300 Completed - Clinical trials for Cesarean Section Complications

Uterine Closure for Cesarean Section: a Novel Technique

Start date: December 1, 2022
Phase:
Study type: Observational

In here we want to describe a new technique to uterin closure at caesarean section which has been performed about 20 years by Bülent Yılmaz. The technique (we suggest the name of the technique as Yılmaz technique) provide less resuturing need when closing the uterus in cesarean section, bringing together better wound edges, providing more effective suture in thin uteruses, stopping active bleeding areas with the same suture, thus enabling to complete the surgery at low cost by using a single suture material in almost all cases. The aim of this study is to describe the technique and compare the blood loss of patients in caserean section between Yılmaz technique and single layer continue locked suturation .

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: NCT04076904 Completed - Clinical trials for Cesarean Section; Dehiscence

Cesarean Niche Examination by Transvaginal us

Start date: October 1, 2019
Phase:
Study type: Observational

The developed uterine scar developing due to cesarean section is usually clinically evaluated and visualized by transvaginal sonography (TVS) and saline infusion sonography (SIS) or Gel installation sonography (GIS)

NCT ID: NCT04070118 Completed - Clinical trials for Cesarean Section Complications

Lower Uterine Segment Thickness and Term Pain,Previous Cesarean Section

Start date: January 1, 2019
Phase:
Study type: Observational

the purpose of the researchers; The aim of this study is to evaluate the consistency of niche dimensions measured by ultrasonography with visual measurement of the surgeon during the operation of the patient when presenting with pain in her current pregnancy. If patients who have had previous cesarean section present to the emergency department with pain or NST pain, a panic occurs immediately for operation. Purpose of researchers; The aim of this study is to investigate whether a really fine determination of the thickness of the old incision line is associated with full-thickness rupture or incomplete rupture, which appears to be an operation, and if a relationship is found, there is a limit for this thickness.

NCT ID: NCT04046783 Completed - Wound Heal Clinical Trials

Patch With Onion Extract and Allantoin for C-section Scar

Start date: March 2, 2019
Phase:
Study type: Observational

The wound healing is a process occurring in response to dermal injury. The resulting scar may have various characteristics ranging from fine-line and asymptomatic to hypertrophic scars and keloids. Prevention or early treatment of pathological scars is the most appropriate approach. Among available remedies, gels and patches containing onion extract and allantoin have been demonstrated to be safe and effective in patients with scars of various origins and severity. One of the most used natural products is a patch containing allium cepa and allantoin licensed for treatment of the scars including keloids. However, up to date, no controlled studies have evaluated the effects of such a device in women who have undergone Cesarean delivery. Therefore, the aim of this study was to investigate the effects of this patch on Cesarean section (C-section) scars.

NCT ID: NCT03859258 Completed - Clinical trials for Cesarean Section; Dehiscence

Ultrasound Based Study For Niche Development In The Uterine Cesarean Section Scar

Start date: July 1, 2017
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to evaluate different factors affecting niche development in the uterine cesarean section scar in women enrolled 3 to 6 months after cesarean delivery using both TVS and SIS.

NCT ID: NCT03629028 Completed - Clinical trials for Cesarean Section Complications

Single or Double-layer Uterine Closure Techniques

Start date: August 18, 2018
Phase: N/A
Study type: Interventional

There are different surgical techniques of uterine closure during cesarean. A growing data has suggested that the closure technique has an effect on uterine scar healing. Residual myometrium thickness and uterine scar defect (niche) development seems to be related to the single or double layer closure of uterus. In that study, investigators will search for the effect of single or double layer closure of uterus during cesarean on the uterine scar defect.