Skip to main content
Clinical Trials/IRCT2016082819470N44
IRCT2016082819470N44
Completed
Phase 2

Comparison of depth of anesthesia in induction with sodium thiopental & propofol in elective cesarean section by BIS, IFT

Vice Chancellor for Research, Shiraz University of Medical Sciences0 sites90 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
caesarean section.
Sponsor
Vice Chancellor for Research, Shiraz University of Medical Sciences
Enrollment
90
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Vice Chancellor for Research, Shiraz University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • 90 pregnant women (ASA I\- II) who are under general anesthesia for elective cesarean section. Exclusion criteria: Patients who are not properly cooperate; patients who received magnesium sulfate MgSO4 before the study; mental disorders; Patients who have a history of previous awareness during general anesthesia, patients who take blood pressure medication or patients who require the use of vasodilators or vasodepressor drugs; patients who consume human stimulant or psychotropic drugs; mothers with multiple gestation or preterm labor; fetal distress, patients with neuromuscular diseases, opium addicts; history of multiple drug allergies or sensitivity to anesthetics; patients with bradycardia and heart block.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Similar Trials