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Phenylephrine and Hypotension During Spinal Anesthesia for Cesarean Section

Anesthesia, Spinal Clinical Trial

Official title:
A Study Evaluating Hypotension and Autonomic Nervous System Dysfunction During Spinal Anesthesia for Cesarean Section and Its Relation to the Effect of Prophylaxis Phenylephrine

Clinical Trial Summary

Pregnant women with a positive preoperative Supine stress test were found to be a subgroup at increased risk of symptomatic hypotension after spinal anesthesia

Clinical Trial Description

Patients will be placed in dorsal decubitus dislocating the uterus to the left for a few minutes, with blood pressure and heart rate recorded three times, with a three-minute interval between measurements to obtain mean baseline levels and this will be repeated in an upright position to record the same measurement.Orthostatic hypotension (Orthostatic hypotension "OH" is defined specifically as a 20mmHg drop in systolic, and/or a 10mmHg drop in diastolic blood pressure within 3 minutes of standing. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02958215
Study type Interventional
Source Assiut University
Contact
Status Completed
Phase Phase 2
Start date June 2016
Completion date May 2017
View Details
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