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Cesarean Delivery clinical trials

View clinical trials related to Cesarean Delivery.

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NCT ID: NCT03026647 Withdrawn - Clinical trials for Cesarean Section; Complications, Wound, Hematoma

Suture Material for Closure of Hysterotomy

Start date: January 31, 2017
Phase: N/A
Study type: Observational

Retrospective chart review evaluating different suture types on surgical outcomes for cesarean delivery and vaginal birth after cesarean delivery outcomes when different sutures are used.

NCT ID: NCT03016273 Recruiting - Cesarean Delivery Clinical Trials

Bladder Flap Technique In Elective Cesarean Section

Start date: February 20, 2017
Phase: N/A
Study type: Interventional

Cesarean section is a surgical procedure used to deliver one or more babies. cesarean section is usually performed when vaginal delivery will put the mother or child's health or life at risk. In recent years, the number of cesarean section has risen worldwide.

NCT ID: NCT02976311 Completed - Inflammation Clinical Trials

Comparison of Inflammatory Responses Subsequent to Different Cesarean Section Techniques

C/S
Start date: April 2016
Phase: N/A
Study type: Interventional

In this study, the investigators aimed to find out whether there are any differences in inflammatory reactions occured subsequent to two different cesarean delivery techniques; modified Misgav-Ladach vs Pfannenstiel-Kerr techniques.

NCT ID: NCT02846129 Completed - Anesthesia Clinical Trials

Incidence of Complications Associated With Anesthesia in Multiple Gestation Undergoing Cesarean Delivery

Start date: October 2016
Phase: N/A
Study type: Observational

Incidence of anesthesia related complications in multiple gestation patients undergoing cesarean delivery has not been reported in Thailand. The aim of this study is to identify complications that occur which may derived from different anesthetic techniques used, such as hypotension, uterine atony, postpartum hemorrhage, rate of hysterectomy, blood transfusion and fetal outcome.

NCT ID: NCT02801968 Recruiting - Cesarean Delivery Clinical Trials

Tap Block and Cesarean Delivery: Efficacy and Consumption of Postoperative Drugs

TAPFANS
Start date: April 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of Tap block after cesarean delivery as a component of multimodal analgesia and evaluation of postoperative drugs consumption.

NCT ID: NCT02717637 Completed - Clinical trials for Analgesic Adverse Reaction

Oxycodone in Serum After Postoperative Oral Oxycodone in Caesarean Sections Under Spinal Anesthesia

Start date: February 2016
Phase: N/A
Study type: Observational

All patients undergoing an elective caesarean section under spinal anesthesia will, according to the hospital routines, receive 10 mg oxycodone slow-release tablet when arriving at our postoperative care unit (PACU). Blood samples will be taken at 0 hour, 1 hour, 2 and 6 hours after administration in order to investigate bioavailability.

NCT ID: NCT02715154 Completed - Clinical trials for Cesarean Section, Affecting Fetus or Newborn

Dexmedetomidine for Cesarean Section

Start date: June 2015
Phase: Phase 1
Study type: Interventional

Current cesarean section often chooses spinal anesthesia. And in order to avoid the impact of drugs on the fetus, before the delivery, anesthesiologist generally don't use sedative or analgesic drugs. However, the majority of puerperas would appear nervous, anxiety, fear and other psychological reactions in cesarean section. Although the placental transfer and the foetal metabolism of dexmedetomidine have been reported and the result show no adverse effects on neonates, but the placental transfer of dexmedetomidine in intravertebral anesthesia area was lack of systematical research. This study intends to use of dexmedetomidine in the cesarean section under epidural anesthesia and investigate its effects on the parturients' haemodynamics and the neonates' placental transfer and metabolism.

NCT ID: NCT02642263 Not yet recruiting - Cesarean Delivery Clinical Trials

Effect of the Uterotonic Carbetocin on Acute Post Cesarean-Section Pain

Start date: February 1, 2019
Phase: Phase 4
Study type: Interventional

Carbetocin is an oxytocin agonist used for prevention of postpartum bleeding after cesarean delivery. First studies revealed in 2012 an analgesic effect of carbetocin, compared to its parent substance oxytocin. This study will enroll 78 women undergoing cesarean delivery. In a double-blind, prospective design patients will be either attributed to the oxytocin or the carbetocin study arm. The primary endpoint will be the area of hyperalgesia around the cesarean delivery scar. This will be performed with a von Frey hair, resulting in a unpleasant feeling in the area of hyperalgesia.

NCT ID: NCT02639429 Completed - Obesity Clinical Trials

Cervical Ripening for Obese Women: A Randomized, Comparative Effectiveness Trial

CROWN
Start date: January 2016
Phase: Phase 4
Study type: Interventional

Obese pregnant women (BMI ≥ 30 kg/m2) are more likely than their normal-weight counterparts to require induction of labor because of increased rates of obstetric complications including pregnancy related hypertensive disorders, diabetes, and prolonged gestations. Several studies have shown that obese women experience increased labor duration and oxytocin needs when compared to normal-weight women. This in turn results in increased rates for unplanned cesarean delivery (CD) as a result of failed induction of labor (IOL), arrest disorders and non-reassuring fetal heart rate tracing, that is dose-dependent with increasing class of obesity. The investigators hypothesize that obese pregnant women and unfavorable cervix (Bishop score ≤ 6), IOL ≥ 24 weeks gestation using the Foley balloon plus vaginal misoprostol will result in reduced cesarean delivery rates when compared to vaginal misoprostol alone.

NCT ID: NCT02129894 Unknown status - Clinical trials for Cesarean Section Post Operative Management

The Use of Abdominal Binders in Patients Undergoing Cesarean Sections

Start date: November 2013
Phase: Phase 3
Study type: Interventional

To see if the use of Abdominal Binders improves patients out comes after cesarean delivery