Comparison of two regimens of total intravenous anaesthesia for time to recovery from anaesthesia.
Not Applicable
- Registration Number
- CTRI/2021/02/030967
- Lead Sponsor
- ADY HARDINGE MEDICAL COLLEGE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA I and ASA II
2.Undergoing elective surgery of duration 1-4 hours
Exclusion Criteria
1.Any known allergy to drugs used in the study.
2.Known psychiatric illness.
3.Narrow angle glaucoma.
4.Addiction to drugs and alcohol.
5.Chronic opioid therapy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time taken to achieve Modified Aldrete Score of �9 (Mean±SD) using propofol with ketamine or dexmedetomidineTimepoint: postoperative every minute till Modified Adrette Score is more than or equal to 9
- Secondary Outcome Measures
Name Time Method 1.haemodynamic complications (bradycardia, tachycardia, hypotension, hypertension) <br/ ><br>2.Mean Bi-spectral index <br/ ><br>3.Total propofol requirement (mcg/kg/min; Mean dose±SD) <br/ ><br>4.Total 24hrs analgesic requirement <br/ ><br>5.post-operative nausea and vomiting <br/ ><br>6.irrelevant talk, hallucination <br/ ><br>7.explicit recallTimepoint: intraoperative haemodynamics every 5 minutes and BIS every 10 min <br/ ><br>At the end of surgery and 24 hours postoperative