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Cesarean Section; Dehiscence clinical trials

View clinical trials related to Cesarean Section; Dehiscence.

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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: NCT03936309 Recruiting - Scar Clinical Trials

A Comparison of Scar Infiltration, Scar Deactivation, and Standard of Care for the Treatment of Chronic, Post-Surgical Pain After Cesarean Section

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

To compare scar infiltration with 0.5-1% Lidocaine at a dose of 3 mg/kg (max dose 300 mg) or scar deactivation with acupuncture surface release technique to determine which is more effective in reducing pain in adult patients with chronic, post-surgical pain related to the site of incision after low transverse Cesarean section compared to standard of care physical therapy with the McKenzie Method.

NCT ID: NCT03911622 Not yet recruiting - Clinical trials for Cesarean Section; Dehiscence

Mri in Evaluation of Cesarean Section Scar Niche

Start date: April 30, 2019
Phase:
Study type: Observational

To evaluate cesarean section scar and the lower uterine segment in non pregnant woman by MRI to : 1. Assess the clinical symptoms like postmenstrual spotting or prolonged menstrual bleeding, dysmenorrhea, chronic pelvic pain and dyspareunia and its relation to the presence of cesarean scar defects and its characteristics . 2. development of scoring system and correlating it with the symptoms .

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: NCT03829774 Recruiting - Clinical trials for Cesarean Section; Dehiscence

To Study and Evaluate the Effectiveness of Treatment by Percutaneous Electrical NeuroStimulation (PENS) for Post-operative Pain in Cesarean Section Patients Using Primary Relief v 2.0

POPS
Start date: January 2, 2019
Phase: N/A
Study type: Interventional

To study and evaluate the Effectiveness of Treatment by Percutaneous Electrical NeuroStimulation (PENS) for post-operative pain in Cesarean Section patients using First Relief

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.

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.