Comparative analysis in dose requirement of propofol for induction of anaesthesia at varying time intervals after fentanyl administration - a Randomized clinical trial
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/07/043932
- Lead Sponsor
- Chettinad Hospital and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 108
Inclusion Criteria
1) Adult patients aged between 18 and 65 years
2) ASA-I & II physical status
3) Elective procedures under general anaesthesia
Exclusion Criteria
1) Patient not willing to be in the study group
2) Contraindication to GA
3) ASA-III & IV physical status
4) BMI > 35 kg/m2
5) Anticipated difficult airway
6) Pregnant patients
7) History of allergy to study drug
8) Drug abuse including chronic alcoholics
9) Emergency procedures
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method