Study to compare the effectiveness of heavy levobupivacaine and heavy Bupivacaine in spinal anaesthesia for lower abdominal and lower limb surgeries
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/071082
- Lead Sponsor
- D Y Patil Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patient undergoing abdominal and lower limb surgeries under spinal anaesthesia
2.ASA 1 and 2
Exclusion Criteria
1.Known hypersensitivity to amide local anaesthetics
2.Contraindications for spinal anaesthesia
3.Bleeding disorders or on anti-coagulant therapy , documented neuromuscular therapy
4.Any infection at the injection site
5.Any spinal deformity
6.Pregnant patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the clinical efficacy of hyperbaric bupivacaine 0.5% and hyperbaric levobupivacaine 0.5% in spinal anaesthesia based on onset of motor blockTimepoint: every 2 mins for first 20mins followed by every 10mins till 60mins then every 30mins till 180mins
- Secondary Outcome Measures
Name Time Method Time taken for complete motor blockade , onset of sensory blockade, duration of sensory and motor blockade and hemodynamic parametersTimepoint: every 2 mins for first 20mins followed by every 10mins till 60mins then every 30mins till 180mins