Comparing how patients recover from laparoscopic surgery when given either propofol or sevoflurane to maintain anesthesia adjusted by the Bispectral Index
Not Applicable
- Registration Number
- CTRI/2024/07/071195
- Lead Sponsor
- ESIC Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
all male and female of ASA grade one and two undergoing elective laparoscopic procedure under general anesthesia
Exclusion Criteria
Patients with known allergy to propofol and sevoflurane and obesity BMI more than or equal to 30 kg per meter square and surgical duration more than two hours
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method