To evaluate effect of dexmedetomidine versus lidocaine on post operative analgesia in spine surgery
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/09/046008
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient undergoing spine surgery with duration within 3 hrs.
ASA Grade I&II.
Weight 40-80 kg.
written and informed consent.
Exclusion Criteria
Patients with a known history of hepatic disese, renal dysfunction, hypertension, atrioventricular block.
history of hypersensitivity to study medication
Patients having chronic pain or concomittantly taking clonidine, methyldopa, beta blockers, benzodiazapines.
Patients having unstable Haemodynamic parameters.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method