A study to evaluate the dose of propofol for general anaesthesia considering the weight of the patient
- Conditions
- Health Condition 1: null- ASA I & II patients, between age group18-60yrs with BMI (30-40kg/m2), undergoing elective laparoscopic surgery under general anaesthesia for atleast 30 minutes and maximum of 3 hours
- Registration Number
- CTRI/2017/10/010044
- Lead Sponsor
- Dr L H Hiranandani Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Patients undergoing elective laparoscopic surgery with BMI between 30 and 40, ASA 1and 2 under general anaesthesia for a minimum duration of 30 minutes to maximum of 3 hours
1.History of significant cardiac pulmonary, liver or renal disease.
2. Patient scheduled for awake bronchoscopic intubation.
3. Previous history of cerebrovascular accident, other neurological disorders and those on long term drugs affecting CNS (chronic BZDâ??s/ opioids)
4. Allergy to propofol.
5. Patients with significant hemodynamic changes intraoperatively, fall of Mean arterial blood pressure by more than 20% of baseline,intraoperative entropy of more than 60 for more than 10 minutes and need to add inhalational agent will be excluded.
6) patients refusal to be included in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method