To find relationship between baseline perfusion index with hypotension following propofol inductio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/03/050904
- Lead Sponsor
- ABVIMS and Dr RML Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients undergoing elective surgery under general anesthesia
2. ASA 1 and ASA 2 patients
3. Age 18 to 65 years
Exclusion Criteria
1. Patients refuse to give consent to get enrolled
in the study
2. ASA 3 and ASA 4 patients
3. Patients undergoing emergency surgery
4. Patients with cardiovascular diseases or taking
any vasoactive drugs
5. Pregnant women
6. Age less than 18 years and more than 65years
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Baseline perfusion index in patients who had hypotension and who did not have hypotension at 5 minutes after Propofol inductionTimepoint: During start of induction with Propofol and 5 minutes after induction
- Secondary Outcome Measures
Name Time Method Cut off value of baseline Perfusion index that can differentiate patients who have hypotension and do not have hypotensionTimepoint: During 5 minutes after induction