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Cesarean Section clinical trials

View clinical trials related to Cesarean Section.

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NCT ID: NCT03114332 Completed - Cesarean Section Clinical Trials

Subcutaneous Drains And Cesarean Section

Start date: December 2015
Phase: N/A
Study type: Interventional

A randomized controlled trial that aimed at studying the values (if any) of subcutaneous drains use in lean women during Cesarean section.

NCT ID: NCT03008577 Completed - Cesarean Section Clinical Trials

Hypothermia and the Effect of Ambient Temperature 2

HEAT2
Start date: August 2016
Phase: N/A
Study type: Interventional

Neonatal hypothermia is associated with increased risk of mortality as well as multiple morbidities. The prior HEAT study conducted at our institution showed a difference in neonatal hypothermia with a change in ambient operating room temperature. The investigator's objective is to determine if an increase in ambient operative room temperature decreases the rate of neonatal morbidity. Operating room temperature will be randomized to the current institutional standard of 20°C (67°F) or a temperature of 24°C (75°F), on a weekly basis for a period of 1.2 years.

NCT ID: NCT03006042 Completed - Anesthesia Clinical Trials

Pharmacokinetics of BPV Following Bilateral US-guided TAP Block for C-section

Start date: November 2014
Phase: N/A
Study type: Observational

The transversus abdominis plane block (TAP block) is an effective method of postoperative pain management after cesarean section (C-section). Up to now, there are no data available about bupivacaine (BPV) plasma levels after TAP block in adults. In the current study, the investigators aimed to assess BPV pharmacokinetic parameters after ultrasound-guided TAP block using BPV in parturients undergoing C-section and to report its effects on corrected QT interval.

NCT ID: NCT03002636 Completed - Cesarean Section Clinical Trials

Safety and Risk Assessment of Obese Parturient Underwent Cesarean Section(CS) Delivery Under Different Anesthesia Ways

Start date: January 2013
Phase: N/A
Study type: Interventional

900 parturient who underwent CS under general anesthesia(GA) , intraspinal anesthesia included epidural anesthesia(EA) and combined spinal-epidural anesthesia(CSEA), which were divided into 3 groups: Morbid Obesity group (n=300) with body mass index (BMI) >40 kg/m2 , severe Obesity group (n=300) with 30 kg/m2≤BMI ≤40 kg/m2 and non-Obesity group(n=300) with BMI<30 kg/m2. Findings Between January 1, 2013 and September 30, 2016, a total of 1000 women met inclusion criteria and 900 women received allocated intervention. All patients were divided into three groups: Morbid Obesity group(n=300), Severe Obesity group(n=300) and non-Obesity group(n=300) according to body mass index (BMI) >40 kg/m2, 30 kg/m2≤BMI ≤40 kg/m2 and BMI<30 kg/m2.900 patients completed the protocol and related data were analysed.

NCT ID: NCT02987803 Completed - Cesarean Section Clinical Trials

Helping Mothers Select Better Childbirth Hospitals

Start date: August 15, 2019
Phase: N/A
Study type: Interventional

The investigators aim to conduct a randomized controlled trial of women who are pregnant or considering pregnancy to understand whether women provided with specific data on hospital-level cesarean delivery rates are more likely to select higher quality hospitals, defined as hospitals with cesarean delivery rates below the Federal HealthyPeople 2020 target of 23.9%.

NCT ID: NCT02977871 Completed - Cesarean Section Clinical Trials

Bladder Flap Versus Omission of Flap During Cesarean Section of Primiparous Women

Start date: July 2016
Phase: N/A
Study type: Interventional

Cesarean section is the most common surgical procedure performed on women. Over the years minor variations of each surgical step have been introduced, and cesarean sections are not standardized and many different techniques are employed during surgery. Creation of a bladder flap has been an integral surgical step of the cesarean section for many years. The role of the bladder flap and its usefulness in cesarean section is not known well. Further, in some cases the bladder flap is omitted during cesarean section. The aim of the current study is to compare operating time and postoperative urinary symptoms in cesarean sections using either bladder flap or omission of flap.

NCT ID: NCT02962011 Completed - Cesarean Section Clinical Trials

Trial Comparing Barbed and Non-barbed Suture for Uterine Incision Closure at Cesarean Section

barbed
Start date: August 1, 2016
Phase: Phase 3
Study type: Interventional

This was an unblinded randomized controlled trial. Women were randomized to uterine closure with the knotless barbed suture (Stratafix PDS, Ethicon) or Vicryl (Ethicon) at the time of elective cesarean. The primary outcome was closure time of the uterine incision. Also measured were blood loss during incision closure and the use of additional hemostatic sutures. Informed consent was obtained

NCT ID: NCT02961842 Completed - Cesarean Section Clinical Trials

Combined Colloid Preload And Crystalloid Coload Versus Crystalloid Coload During Spinal Anesthesia for Cesarean Delivery

Start date: November 20, 2016
Phase: N/A
Study type: Interventional

The study will compare one technique of fluid administration (combined colloid preload and crystalloid colaod) with another one (crystalloid coload) during elective cesarean delivery performed under spinal anesthesia.

NCT ID: NCT02956616 Completed - Cesarean Section Clinical Trials

Enhanced Recovery at Cesarean Birth to Improve Postoperative Outcomes and Reduce Postoperative Length of Stay

ERAC
Start date: September 1, 2017
Phase: Phase 2
Study type: Interventional

To determine whether women randomized to an enhanced recovery program will have improved postoperative outcomes including improved breastfeeding initiation and continuation, reduction in hospital length of stay without compromising patient satisfaction in comparison to standard postoperative recovery interventions.

NCT ID: NCT02899260 Completed - Cesarean Section Clinical Trials

Using the Peanut Exercise Ball to Reduce Cesarean Section Rates: A Randomized Controlled Trial

Start date: August 2016
Phase: N/A
Study type: Interventional

This study is designed as a prospective, randomized controlled trial that will compare the use of the peanut exercise ball in laboring patients compared with no use of the exercise ball. We hypothesize that use of the peanut ball decreases the incidence of cesarean section.