A study to Compare Different Anesthetic agents as a cause of Delirium after ECT
Not Applicable
- Conditions
- Health Condition 1: F30-F39- Mood [affective] disordersHealth Condition 2: F20-F29- Schizophrenia, schizotypal, delusional, and other non-mood psychotic disorders
- Registration Number
- CTRI/2023/01/049228
- Lead Sponsor
- Government Medical College Kota
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients above 18 years of age.
2. Patients whose informed consent has been obtained.
3. Only the first session of ECT during current admission of the patient will be studied.
Exclusion Criteria
1. Patient who have received ECT during the last one year.
2. Patients with clinically significant laboratory abnormality or ECG findings.
3. Patients with delirium.
4. Patients with organic or neurological disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The role of thiopental, propofol, etomidate on Post- ECT delirium and recovery.Timepoint: Patient alertness will be assessed using Richmond Agitation- Sedation Scale and delirium with Confusion Assessment Method for the ICU at 15 min, 30 min and 1 hour after eye opening.
- Secondary Outcome Measures
Name Time Method To identify predictors of Post ECT delirium and recovery. <br/ ><br> <br/ ><br>Timepoint: Predictors of Post Electroconvulsive therapy delirium