A study to evaluate how effective it is to add Sufentanil to Propofol in intravenous anaesthesia for patients undergoing laparoscopic cholecystectomy
Phase 4
Completed
- Registration Number
- CTRI/2008/091/000182
- Lead Sponsor
- DrM Subrahmanyam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Adult patients aged between 18 and 65 years of both sexes, of American Society of Anaesthesiologists (ASA) physical status I or II with airway status - Mallampati scores 1 and 2, posted for elective laparoscopic cholecystectomy
Exclusion Criteria
Age less than 18 years or more than 65 years, body weight more than 90 kgs, ASA physical status III to V, Mallampati scores 3 and 4 of airway, history of hypertension, history of coronary artery disease, history of long term analgesic use, history of psychiatric disorders, patients with severe hepatic or renal dysfunction and patients in whom NSAIDS are contraindicated.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perioperative haemodynamic parameters: Heart rate, systolic blood pressure and diastolic blood pressureTimepoint: During the peri-operative period at different time intervals: pre-induction or baseline, postinduction 1 minute, postinduction 3 minutes, postinduction 5 minutes, Intraoperative 15 minutes, Intraoperative 30 minutes, Intraoperative 45 minutes, Intraoperative 60 minutes, Intraoperative 75 minutes, Intraoperative 90 minutes, Intraoperative 105 minutes, Post-extubation 1 minute, Post-extubation 5 minutes.;post-operative analgesiaTimepoint: From the end of anaesthesia upto 24 hours postoperatively;Recovery time from anaesthesiaTimepoint: Towards the end of anaesthesia for each patient undergoing surgery
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI