To estimate the concentration of propofol achieved in brain during anesthesia using a software.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- ASA 1 and 2 patients coming for surgery.
- Registration Number
- CTRI/2018/03/012491
- Lead Sponsor
- Institute Research Grant
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 35
Inclusion Criteria
•ASA 1 & 2
•Elective surgery duration < 2 hrs.
Exclusion Criteria
1. Patients with CNS disorders and head injury
2. Pregnant women
3. Allergy to administered drugs
4. Body mass index more than 25.
5. Difficult airway
6. Drug or alcohol abuse
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method