ow-dose ketamine infusion during laparoscopic surgery for postoperative pain relief
Phase 2
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/11/022120
- Lead Sponsor
- Pondicherry Institute Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 52
Inclusion Criteria
General surgical patients aged 18 to 60 years belonging to American society of anaesthesia (ASA) I and II posted for laparoscopic surgeries.
Exclusion Criteria
1.Patients on chronic analgesic medication
2.Any known contraindication to the study drug
3.Patients with BMI > 30 kg/m2
4.Uncontrolled hypertension, raised intraocular pressure/glaucoma
5.Emergency surgery
6.Psychiatric patients
7.Pregnant women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determination of the efficacy of low dose Ketamine for postoperative pain relief in laparoscopic surgeries.Timepoint: 6 hours
- Secondary Outcome Measures
Name Time Method To study and compare haemodynamic parameters intraoperatively between the two groups. <br/ ><br> <br/ ><br>Timepoint: 6 hours;To study and compare the frequency and amount of opioid requirement postoperatively between the two groups.Timepoint: 6 hours;To study the occurrence of complications like hallucinations, sedation, vomiting, if any postoperatively. <br/ ><br> <br/ ><br>Timepoint: 6 hours