A clinical trial to study intraoperative blood glucose level changes between obese and non-obese non-diabetic patients undergoing craniotomy surgery under general anaesthesia
Not Applicable
Completed
- Conditions
- Health Condition 1: null- changes in perioperative BLOOD GLUCOSE levels
- Registration Number
- CTRI/2018/03/012821
- Lead Sponsor
- Department of Anaesthesiology Bangur Institute of Neurology IPGMER SSKMH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
1. ASA physical status I and II
2. non-diabetic obese patients undergoing craniotomy surgery under general anaesthesia
3. non-diabetic non-obese patients undergoing craniotomy surgery under general anaesthesia
Exclusion Criteria
1. unwilling patients
2. patients with severe cardiovascular, respiratory, renal and endocrine disease including diabetes mellitus
3. all emergency surgeries
4. surgeries other than neurosurgical procedures
5. operations under regional anaesthesia
6. hemodynamically unstable patients
7. pregnancy
8. ASA physical status III or more
9. age <18 yrs and >65 yrs
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method blood glucose level changes will be more in obese than in non-obese population and the change will increase with the duration of surgeryTimepoint: preoperative single value, just after induction of anaesthesia and thereafter at half an hour interval till the end of operation, single value postoperatively 30 minutes after extubation
- Secondary Outcome Measures
Name Time Method insulin requirement will be more in obese than in non-obese patients and the requirement will increase with the duration of surgeryTimepoint: 180 minutes