Prediction of pain after surgery from pain due to venous cannulation and propofol infusion before surgery.
Not Applicable
- Conditions
- Health Condition 1: null- Patients undergoing elective laparoscopic cholecystectomy.
- Registration Number
- CTRI/2018/03/012616
- Lead Sponsor
- Dr Yatish B
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with American Society of Anaesthesiologists physical status I or II undergoing an elective laparoscopic cholecystectomy.
Exclusion Criteria
1.Patient with history of recurrent preoperative pain
2.Inability to understand instructions
3.Contraindications to the study drugs
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the correlation between preoperative bedside VAS assessments of pain intensity associated with venous cannulation and propofol infusion and postoperative pain estimatesTimepoint: Postoperative pain intensity at rest,will be assessed from arrival in the post-anaesthesia care unit and at 10, 20, 30, 60 and 90 min in awake patients.
- Secondary Outcome Measures
Name Time Method The timing of first rescue dose of morphine and total dose of morphine at the end of 90 minutes.Timepoint: Measures of postoperative pain will be evaluated by pain intensity ratings, time from extubation to first dose of morphine, and total dose of morphine within 90 min.