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Complications; Cesarean Section clinical trials

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NCT ID: NCT02893696 Withdrawn - Hypotension Clinical Trials

Extra Sitting Time After Spinal Anesthesia for Cesarean Section and Fetal Well-being

Start date: March 2018
Phase: N/A
Study type: Interventional

After injection of the spinal anesthetic drug, women will be allowed to lie down immediately (0-30 sec) or after three minutes (180 sec) of sitting. The incidence of maternal hypotension and fetal umbilical cord blood pH will be recorded.

NCT ID: NCT02101047 Withdrawn - Clinical trials for Complications; Cesarean Section

Phenylephrine Dose and Mode of Administration for Spinal Anesthesia Induced Hypotension

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

Three different regimens of phenylephrine are being evaluated to see if one is superior over the other in the maintenance of cardiac output while keeping normotension and/or treating hypotension experienced when receiving spinal anesthesia for cesarean delivery.

NCT ID: NCT01516697 Withdrawn - Clinical trials for Complications; Cesarean Section

Non-invasive Cardiac Output Monitoring in Obstetric Patients

Start date: October 2011
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that continuously measuring stroke volume (SV) and cardiac output (CO) will 1) reveal hemodynamic instability in a timely manner and alert the physician promptly, 2) provide information for the physician to make the differential diagnosis as to whether the hemodynamic instability was due to vasodilatation or reduction of venous blood return, and 3) lead to appropriate and prompt treatment to improve patient outcome. -determine the SV and CO and their kinetic change using ICON® to establish a hemodynamic profile of the patient under spinal anesthesia for cesarean section. To determine if using instantaneous measurements of SV and CO to guide patient management improves hemodynamic stability.