Evaluation the effect of Propofol, Etomidate, and Sodium Thiopental on depth of Anesthesia and duration of Seizure in the electroconvulsive therapy
Phase 2
- Conditions
- Electroconvulsive Therapy.Treatment of depressive episode
- Registration Number
- IRCT2014050617602N1
- Lead Sponsor
- Vice chancellor for research, Ahvaz Jundishapur University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 132
Inclusion Criteria
Admitted patients for Electroconvulsive Therapy in Golestan hospital;
30 to 50 years old;
Anesthesia risk of 1, 2 (According to American society of anesthesiologist's classification).
Exclusion criteria:
Patient refuse;
Under 30 and over 50 years old;
A history of drug abuse;
Sensitivity to egg;
Contraindication of Propofol, Etomidate or Sodium Thiopental.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measuring Depth of Anesthesia. Timepoint: Continuously during procedure. Method of measurement: By bipolar electroencephalographic leads that connected to the temporal and frontal area of patients and brain waves evaluated by BIS monitoring according to numbers from 0 to 100.;Duration of Seizure. Timepoint: After procedure. Method of measurement: Clinical Observation.
- Secondary Outcome Measures
Name Time Method