Comparison of pain relief with Fentanyl(A pain relieving drug) using a numerical scaleas compared to routine method of administration in patients undergoing gall bladder removal surgery.
Phase 2
- Conditions
- Health Condition 1: null- Patients posted for laparoscopic cholecystectomy
- Registration Number
- CTRI/2017/05/008644
- Lead Sponsor
- Dr Neetu Jain MD DNB
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 140
Inclusion Criteria
1. ASA Physical status I and II
Exclusion Criteria
1. Patients with hypersensitivity to any of the drugs to be used
2. Hypertension
3. Weight < 70% or >130% of ideal body weight
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare fentanyl requirement using SPI guided administration versus conventional mode of administrationTimepoint: Intraoperatively
- Secondary Outcome Measures
Name Time Method To determine any difference between the two study groups in: <br/ ><br>Haemodynamic events <br/ ><br>Recovery time <br/ ><br>Quality of postoperative pain relief <br/ ><br>Postoperative nausea and vomiting <br/ ><br>Respiratory depression <br/ ><br>Timepoint: Intraoperatively and Postoperatively 15 minutes after shifting to recovery.