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

Phase 2

• Conditions: caesarean section.; Delivery by elective caesarean section

• Registration Number: IRCT2016082819470N44
• Lead Sponsor: Vice Chancellor for Research, Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 90

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To determine the depth of the anesthesia bySodium Thiopental and Propofol as an induction anesthetic. Timepoint: at baseline, Induction of anesthesia, laryngoscopy and intubation, Skin incision, opening the peritoneum, Uterine incision, childbirth Uterine closure, , tying the layers under the skin, Subcutaneous closures, skin closure, turn off the gas anesthesia, eye opening and extubation. Method of measurement: bispectral index (BIS) and Isolated forearm technique (IFT).