A clinical trial to study the effects of two drugs, propofol and etomidate on blood pressure, seizure duration, and recovery profile during electro - convulsive therapy.
Not Applicable
- Conditions
- Health Condition 1: G978- Other intraoperative and postprocedural complications and disorders of nervous system
- Registration Number
- CTRI/2019/03/018031
- Lead Sponsor
- SVIMS University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I,â?¡ psychiatric patients who will undergo consecutive electroconvulsive therapies between age 18- 60 years
Exclusion Criteria
H/O recent myocardial infarction, recent cerebrovascular accident
Angina Pectoris
Congestive Heart Failure
Major Bone Fractures
Pregnancy and lactation
Aneurysms of major vessels
Porphyria
Patients with shock and hypovolemia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To analyse the blood presuure, heart rateTimepoint: 2 months
- Secondary Outcome Measures
Name Time Method To study seizure duration and recovery profile in patients undergoing ECTTimepoint: 6 months