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A study to compare the machine controlled with human controlled changes in propofol dose for patients undergoing laproscopic cholecystectomy under general anaesthesia

Not Applicable
Conditions
Health Condition 1: - Health Condition 2: K800- Calculus of gallbladder with acutecholecystitisHealth Condition 3: K802- Calculus of gallbladder without cholecystitis
Registration Number
CTRI/2024/04/065417
Lead Sponsor
Maulana Azad Medical College and associated hospitals
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Age 18 – 65 years

2. ASA physical health status 1 and 2

Exclusion Criteria

1.Cardiac, liver or kidney disease

2. History of drug or alcohol abuse

3. Allergy to Propofol

4. Allergy to egg or soya bean oil

5. Regular intake of sedative or hypnotic or psychiatric medication

6. Obesity (BMI >30kg/m2)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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