Clinical Trials Directory

Trials / Completed

CompletedNCT02958215

Phenylephrine and Hypotension During Spinal Anesthesia for Cesarean Section

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

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
980 (actual)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGPhenylephrineit will be given as a prophylaxis for prevention of hypotension after spinal anesthesia in pregnant patients undergoing cesarean section
OTHERPlacebo5 ml normal saline will be given before spinal anesthesia

Timeline

Start date
2016-06-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2016-11-08
Last updated
2017-05-18

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02958215. Inclusion in this directory is not an endorsement.