The study compares using brain activity measurements and the loss of verbal response to decide how much propofol should be given for anesthesia in adult patients undergoing elective surgeries. The research randomly assigned participants to different groups.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063833
- Lead Sponsor
- KUSHAL YALABURGI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age 18 to 60 YEARS
2. Patient willing to give informed consent and procedure as per the declaration of Helsinki guidelines
3. American society of Anesthesiologist Physical Status : ASA 1,2 in patients undergoing elective surgeries under general anaesthesia.
Exclusion Criteria
1. Patients with severe cardiac disease, liver diseases and renal dysfunction.
2. Patients not willing to give informed consent.
3. Emergency procedures.
4. Patients with hearing disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.The dose of propofol required for induction of general anesthesia, as determined by EEG entropy and loss of verbal response.Timepoint: during induction of anaesthesia
- Secondary Outcome Measures
Name Time Method 2.Incidence of adverse events, such as hypotension, bradycardia during induction of anesthesia.Timepoint: one, five & 10 mins after induction of anaesthesia