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Obstetric Labor Complications clinical trials

View clinical trials related to Obstetric Labor Complications.

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NCT ID: NCT03719625 Not yet recruiting - Cesarean Clinical Trials

Norepinephrine Versus Ephedrin for Prevention of Post Spinal Anesthesia in Cesarean Section

Start date: January 2, 2019
Phase: Phase 4
Study type: Interventional

Spinal anesthesia is still the gold standard anesthetic method for elective and urgent cesarean section, the post spinal hypotension remains the most frequent complication of this procedure and is still responsible of considerable maternel and fetal morbidity. It is recommanded to prevent this post spinal hypotension with fluid coloading and prophylactic vasopressors administration. The aim of this study is to compare the efficency and the safety of norepinephrin and ephedrin prophylactic administration to reduce the incidence of post spinal hypotension in cesarean section.

NCT ID: NCT02759510 Not yet recruiting - Clinical trials for Hemodynamic Instability

Cardiac Output Changes in Cesarean Section

Start date: June 2016
Phase: Phase 0
Study type: Interventional

Since 2011, phenylephrine was recommended as the preferred drug to maintain blood pressure in obstetric anesthesia.Phenylephrine, an α adrenoceptor agonist, can induce peripheral vasoconstriction to maintain blood pressure, while reflexly decrease heart rate and result in cardiac output (CO) reduction.Norepinephrine acts not only as an α adrenoceptor receptor agonist, but also as a weaker β adrenergic receptor agonist. It can elevate blood pressure the same asphenylephrine, meanwhile produce positive inotropic effect including increasing heart rate.Thus, the administration of norepinephrine can maintain blood pressue and avoid the decline of CO. The purpose of this study is to evaluate the effect of norepinephrine and phenylephrine on maternal CO in cesarean section by transesophageal echocardiography.

NCT ID: NCT02223949 Not yet recruiting - Obesity Clinical Trials

Labor Induction and Maternal BMI, Comparison of Different Pre-induction Cervical Ripening Methods

Start date: October 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate whether mechanical cervical ripening (using the Cook double balloon catheter) is superior or inferior to pharmacological agents (PGE1) in overweight and obese women undergoing labor induction.