To study if a smaller dose of propofol given prior to the actual dose will be able to reduce its total dose required.
Not Applicable
- Conditions
- Health Condition 1: K35-K38- Diseases of appendixHealth Condition 2: H65-H75- Diseases of middle ear and mastoidHealth Condition 3: K80-K87- Disorders of gallbladder, biliary tract and pancreasHealth Condition 4: K40-K46- HerniaHealth Condition 5: C73-C75- Malignant neoplasms of thyroid and other endocrine glands
- Registration Number
- CTRI/2020/06/025742
- Lead Sponsor
- REEHANA JABARULLA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 and 2
Exclusion Criteria
H/O allergy to egg, opioids
Alcoholics
H/O intake of CNS depressants
ASA 3 and 4
Haemodynamic instability
BMI > 35
Anticipated difficult intubation
Pregnancy and lactating mothers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To Study the Effect of Priming Principle on the Induction dose requirement of Propofol.Timepoint: 1 year
- Secondary Outcome Measures
Name Time Method To Compare the Hemodynamics between the group in which Priming Principle was applied and the group in which No priming was applied. <br/ ><br> <br/ ><br>Timepoint: 1 year