Comparison of the effects of Ketamine and Propofol and Dexmedetomidine in treatment with electroconvulsive therapy in patients with depressio
Phase 3
Recruiting
- Conditions
- Schizophrenia.Schizophrenia
- Registration Number
- IRCT20141209020258N143
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
18 to 60 years
Both sexes
Patients with a diagnosis of schizophrenia
Exclusion Criteria
No history of drug use
No pregnancy
No history of cardiovascular disease (arrhythmias, ischemia, heart block)
Do not take beta-blockers
There are no contraindications to ECT, such as spinal cord injury and high ICP, and recent heart attacks.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate. Timepoint: Every 5 minutes. Method of measurement: Counting.;Mean blood pressure. Timepoint: Every 5 minutes. Method of measurement: Barometer.;Seizure duration. Timepoint: In times of seizures. Method of measurement: Minutes.;Patient satisfaction. Timepoint: After the shock. Method of measurement: Satisfaction Questionnaire.;Recovery duration. Timepoint: After the shock. Method of measurement: Minute.
- Secondary Outcome Measures
Name Time Method