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Cesarean Section Complications clinical trials

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NCT ID: NCT03224247 Enrolling by invitation - Clinical trials for Cesarean Section Complications

Vertical Splitting of Muscle Layer in Lower Segment Cesarean Sections to Avoid Uterine Vessels Injury

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Cesarean section is one of the oldest surgical interventions in the history of medicine.Many variations in cesarean section technique have been studied.The investigatory team are aiming to decrease blood loss during cesarean section by vertical splitting versus transverse cutting of muscle layer in lower segment cesarean sections to avoid uterine vessels injury.

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: NCT03182088 Completed - Clinical trials for Cesarean Section Complications

Norepinephrine Infusion Different Doses in Cesarean Delivery

Start date: June 15, 2017
Phase: Phase 4
Study type: Interventional

three doses (0.025 mcg/Kg/min, 0.050 mcg/Kg/min, and 0.075 mcg/Kg/min) of norepinephrine will be compared for prophylaxis against Post-spinal anesthesia hypotension during Cesarean delivery.

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: NCT03170427 Completed - Clinical trials for Cesarean Section Complications

Impedance Cardiography as Tool for Continuous Hemodynamic Monitoring During Cesarean Section

Start date: January 1, 2013
Phase: N/A
Study type: Interventional

Impedance Cardiography (ICG) is a non-invasive tool for continuous hemodynamic monitoring. Aims of our study is to assess the utility of ICG to evaluate the hemodynamic impact of 6 mg (GL6) vs 8 mg (GL8) levobupivacaine combined with fentanyl in healthy patients undergoing elective cesarean section; secondary, to compare the duration and quality of analgesia and anesthesia

NCT ID: NCT03163407 Completed - Hypotension Clinical Trials

Norepinephrine Versus Ephedrine in Treatment of Hypotension During Spinal Anesthesia for Caesarean Section

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

Prospective, randomized study, including full term parturients scheduled for caesarean section under spinal anesthesia. Spinal anesthesia was performed in sitting position with a 25 G spinal needle and all patients received 15 ml/kg of crystalloid intravenously during the spinal block. Baseline hemodynamics: heart rate, systolic and diastolic blood pressure were recorded before spinal anesthesia and intraoperatively. Postspinal hypotension, defined as decrease of Systolic blood pressure>20% from the baseline value, was managed using Ephedrine increments 6 mg/3min in patients of GE group or by 5 mcg Norepinephrine/3min for the patients of GN group. Intraoperative hemodynamic data of the 2 groups were compared.

NCT ID: NCT03115047 Completed - Clinical trials for Cesarean Section Complications

Shivering Treatment After Cesarean Delivery: Meperidine vs. Dexmedetomidine

Start date: May 7, 2017
Phase: Phase 3
Study type: Interventional

Comparing two treatments for shivering after cesarean delivery for labor dystocia under epidural anesthesia.

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: NCT03080506 Completed - Clinical trials for Cesarean Section Complications

Abdominal Binder Following Cesarean Delivery

Start date: April 18, 2017
Phase: N/A
Study type: Interventional

Cesarean delivery is a common obstetrical procedure and is associated with increased maternal morbidity and mortality. Pain and limited mobilization are major contributing factors that result in delayed functional recovery and complications. Elastic abdominal binder, a wide elastic belt that is wore around the patient's abdomen to support surgical incision after surgery, has been employed by clinicians for pain relief, wound complications prevention, improved pulmonary function, and stabilization. Benefits of the abdominal binder use have not been properly examined. The aim of this study is to examine the effect of postcesarean elastic abdominal binder use on recovery by comparing pain scores and mobility function (through the 6-minute walk test [6MWT]) in postcesarean mothers who use versus do not use the elastic abdominal binder to support incisional site.

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.