To Compare The Dose Of Propofol Drug For Induction Of General Anaesthesia As Determined By Entropy Monitoring Against The Standard Induction Dose In Elderly Patients
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/01/048808
- Lead Sponsor
- ot applicable
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients in age group more than 50 years of either sex belonging to American Society of Anesthesiologist 1&2
Exclusion Criteria
1.Patients who have history of allergy to propfol.2.patients with history of cardiac disease.3.ASA 3 and ASA 4 STATUS patients.4.long term use of drugs affecting the central nervous system.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method