OW DOSE INTRAVENOUS KETAMINE AS A PREEMPTIVE ANALGESIC FOR POSTOPERATIVE PAIN MANAGEMENT
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and SurgicalHealth Condition 3: null- Patients undergoing elective surgery under General Anaesthesia
- Registration Number
- CTRI/2018/03/012595
- Lead Sponsor
- Armed Forces Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 77
Inclusion Criteria
1. Age > 12 years
2. ASA Class I, II
Exclusion Criteria
1.Intraoperative or postoperative administration of spinal/epidural anaesthesia or any regional blocks
2.Any severe perioperative complications requiring post op ICU admission
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the efficacy of preemptive administration of low dose intravenous ketamine (0.5mg/kg) in patients undergoing surgery under GA on <br/ ><br>a)Total consumption of opioids (i.e. Tramadol) in first 24 hours postoperatively <br/ ><br>b)Time taken to first demand of rescue analgesia with opioid (i.e. Tramadol) <br/ ><br>Timepoint: 1 hour, 6 hours, 12 hours and 24 hours
- Secondary Outcome Measures
Name Time Method a)To study the efficacy of preemptive administration of low dose intravenous ketamine on postoperative pain scores <br/ ><br>Timepoint: 1 hour, 6 hours, 12 hours and 24 hours