Compare recovery profile of propofol administered by manual infusion with target controlled infusion in gynaecological surgeries
Not Applicable
- Conditions
- Health Condition 1: N839- Noninflammatory disorder of ovary,fallopian tube and broad ligament, unspecified
- Registration Number
- CTRI/2023/03/050936
- Lead Sponsor
- SRM Medical College Hospital and research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients posted for Gynaecological Endoscopic surgeries
2. Age 18 year to 65 year
3. ASA I/II
Exclusion Criteria
1. Non-consenting patients
2. Uncontrolled co-morbid illness
3. Hypersensitivity/allergy to propofol
4. Patients with psychiatric disorders
5. Patients with opioid dependency
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the time taken to recover as assessed by time taken to obey simple <br/ ><br>commands after termination of propofol infusion in both techniquesTimepoint: After end of surgery
- Secondary Outcome Measures
Name Time Method 1. Total dose of propofol administered (mg/kg/hr) <br/ ><br>2. Change in Mean Arterial Pressure (MAP) post-inductionTimepoint: End of surgery