Comparison of two different doses of propofol and its effect on hemodynamic response
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/06/033990
- Lead Sponsor
- Sentila Shangne
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1&2
Elective surgeries under general anaesthesia
Patients with a signed informed written consent form
Exclusion Criteria
Patient refusal
History of cardiac diseases like dilated cardiomyopathy,CCF, Arrhythmias etc
History of uncontrolled hypertension and hypotension
Patients with hepatic or renal dysfunction, pregnancy or any serious medical conditions that would interfere with cardiovascular response
Patients with history of allergy to any GA drugs
Cases lasting less than 30mins
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare sleep guided dose of propofol with BIS guided dose on haemodynamic responseTimepoint: Baseline,15minutes intraoperative and 15minutes postoperatively
- Secondary Outcome Measures
Name Time Method To Assess sedation scaleTimepoint: Postoperative Period upto 48 hrs