Comparison between sedation monitoring devices and clinical parameters for propofol( a drug used to put a patient to sleep for surgery) induction in Indian patients:
Not Applicable
- Conditions
- Health Condition 1: K00-K95- Diseases of the digestive system
- Registration Number
- CTRI/2020/01/022634
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Inclusion criteria would be patients between the age group 18 - 65 years old, both male and female sexes and patients fitting the American society of anaesthesiologist (ASA) physical status I-II
Exclusion Criteria
1. Patient refusal to participate in the study
2. Pregnancy, seizure disorders, bleeding diathesis and conversion into open cholecystectomy due to any reason
3. Severe cardiac, hepatic, renal or metabolic disease
4. Long term drug or alcohol abuse
5. Body weight > 50% above ideal body weight
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Dosage of propofol used for induction of a patient as evaluated by Patient state index (PSI), Bispectral index (BIS) and clinical parameters.Timepoint: One reading intraoperatively on how much is the dosage of propofol used
- Secondary Outcome Measures
Name Time Method 1.Correlation between Patient state index (PSI), Bispectral index (BIS) and clinical parametersTimepoint: Every five minutes till end of surgery