A clinical trial to compare the postoperative pain relieving effect of intraoperative ketamine and fentanyl infusion in major abdominal surgeries
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2018/12/016649
- Lead Sponsor
- AIIMS Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American society of Anesthesiologists physical status 1 and 2
Exclusion Criteria
Patients less than 18 yrs and more than 60 yrs
Patient refusal to participate in the study
Patient with Opioid abuse, long term analgesic use or alcohol consumption
Patient with known allergy or contraindications to any of the drugs used.
Patient converted to open cholecystectomy
Body mass index (BMI) less than 18 kg/m2 greater than 35 kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of effect of intraoperative low dose ketamine and low dose fentanyl on postoperative opioid analgesic requirement in adults undergoing laparoscopic abdominal surgeryTimepoint: Opioid analgesic requirements for 24 hrs
- Secondary Outcome Measures
Name Time Method Assessment of effect of intraoperative low dose ketamine on postoperative VAS scores in adults undergoing laparoscopic abdominal surgeryTimepoint: Post operative VAS scores for 8 hrs;To assess the effect of intraoperative low dose ketamine infusion on time required for extubationTimepoint: From closure of inhalational anaesthetics to extubation time;To assess the presence of side effects of ketamine postoperatively with intraoperative low dose ketamine infusionTimepoint: Assessment for 8 hrs