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Cesarean Section Complications clinical trials

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NCT ID: NCT03355378 Recruiting - Clinical trials for Cesarean Section Complications

Short Versus Standard Post-operative Stay After Elective Cesarean Delivery

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

After major open abdominal surgery, transient paralytic ileus usually follows. It has been suggested that stimulation of pain fibers, excessive sympathetic tone, and the release of inhibitory neurotransmitters from bowel wall associated with bowel manipulation and peritoneal irritation are responsible mechanisms. There have been concerns that early postoperative oral feeding would lead to vomiting with subsequent aspiration pneumonia, anastomotic leakage, and wound dehiscence.

NCT ID: NCT03261765 Recruiting - Clinical trials for Cesarean Section Complications

Effect of Multiple Repeat Cesarean Sections on Intra-abdominal Adhesions

Start date: June 1, 2018
Phase:
Study type: Observational

The rate of cesarean section deliveries has increased dramatically worldwide in the last decades. While the cesarean birth rate was 4.5% in the USA in 1965, it was 31.8% according to 2007 data and is thought to be over 50% at present. The reasons for this include advanced age of primigravida, a wide range of indications, patient requests, the frequency of women with previous cesareans, women's rejections to offers of sterilization, and the common usage of assisted reproductive techniques

NCT ID: NCT03248817 Recruiting - Clinical trials for Cesarean Section Complications

Phenylephrine Infusion in Cesarean Delivery

Start date: September 28, 2017
Phase: Phase 4
Study type: Interventional

the investigators will compare variable infusion of phenylephrine (at a starting rate of 0.75 mcg/Kg/min) with fixed rate (0.75 mcg/Kg/min which will stop of reactive hypertension occurred) and single shot (1.5 mcg/Kg) phenylephrine

NCT ID: NCT03248791 Recruiting - Clinical trials for Cesarean Section Complications

Vasopressor Infusion in Cesarean Delivery

Start date: August 20, 2017
Phase: Phase 4
Study type: Interventional

Comparison will be conducted between continuous variable infusions of both drugs (Phenylephrine and Norepinephrine) with starting doses of 0.75 mcg/Kg/min and 0.1 mcg/Kg/min respectively for prophylaxis against Post-spinal hypotension during cesarean delivery.

NCT ID: NCT03182114 Recruiting - Clinical trials for Cesarean Section Complications

Supine Versus Left Lateral Tilted Position During Cesarean Delivery

Start date: June 12, 2017
Phase: Phase 4
Study type: Interventional

In this study, we will investigate the effect of left lateral tiling performed after spinal block on maternal hemodynamics compared to ordinary supine position

NCT ID: NCT03181776 Recruiting - Clinical trials for Cesarean Section Complications

Hemodynamic Effect of Left Tilting in Cesarean Delivery

Start date: June 22, 2017
Phase: N/A
Study type: Interventional

The aim of this work is to investigate the effect of different angles of lateral tilt on the maternal hemodynamics before and after subarachnoid block

NCT ID: NCT03113045 Recruiting - Clinical trials for Cesarean Section Complications

Seated Time for 90% Incidence of Hypotension

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

The study will determine the 90% effective seated time after intrathecal injection of hyperbaric bupivacaine to avoid hypotension in patients undergoing cesarean delivery.

NCT ID: NCT03070795 Recruiting - Clinical trials for Cesarean Section Complications

Outcomes of Early Versus Delayed Oral Feeding After Cesarean Section in Korle-bu Teaching Hospital

Start date: February 23, 2017
Phase: N/A
Study type: Interventional

study compares the outcomes of feeding mothers early (4 hours ) after cesarean section compared to delayed feeding (on post operation day 1) in terms of gastrointestinal function and maternal satisfaction with the feeding schedule.