CTRI/2023/06/054099
Not yet recruiting
Phase 3
To study the efficacy of Dexmedetomidine as an adjuvant to hyperbaric preparations of 0.5% Levobupivacaine, 0.75% Ropivacaine & 0.5% Bupivacaine in the patients undergoing surgeries under subarachnoid block
Department of Anaesthesia and Critical Care0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: O- Medical and Surgical
- Sponsor
- Department of Anaesthesia and Critical Care
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Consent from patients and ASA grading I\-II posted for lower abdominal and lower limb surgical procedures planned under subarachnoid block.
Exclusion Criteria
- •Non consenting as well pregnant patients, any spinal deformities, infection at the site,uncontrolled co\-existing systemic and metabolic diseases, history of alcohol abuse, known sensivity to any LAAs and dexmedetomidine shall be excluded from the study , patients on beta blockers and sinus bradycardia
Outcomes
Primary Outcomes
Not specified
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