se of two different drungs as adjuvant to levobupivacaine for spinal anaesthesia in lower limb surgeries.
Not Applicable
Completed
- Conditions
- Health Condition 1: S90-S99- Injuries to the ankle and footHealth Condition 2: S70-S79- Injuries to the hip and thighHealth Condition 3: S80-S89- Injuries to the knee and lower leg
- Registration Number
- CTRI/2019/02/017756
- Lead Sponsor
- IMS BH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 135
Inclusion Criteria
ASA Grade 1, 2
Patients scheduled to have various lower limb sugeries.
Exclusion Criteria
Patient who refuse to participate in study.
Patients not opting for subarachnoid block as anaesthetic technique.
Patients with local infection or significant coagulopathy.
Patients with severe cardiopulmonary disease.
Patients with blood volume deficit.
Patients with allergy to local anaesthetics or study drugs.
Patients with long term opioid use.
Patients with Peripheral Neuropathies,scoliosis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of Sensory blockadeTimepoint: Minutes 1,3,5,10,15,20,30 and 60.
- Secondary Outcome Measures
Name Time Method Full recovery of Sensory blockadeTimepoint: Hours 6 and 12.