Efficacy of Unilateral Spinal Anaesthesia using very low drugs and administering drug very slowly.
Not Applicable
- Conditions
- Health Condition 1: null- American Society of Anaesthesiology physical status Grade 1 and 2
- Registration Number
- CTRI/2018/03/012819
- Lead Sponsor
- eena H Parate
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade 1,2
Lower limb surgeries
Exclusion Criteria
Patients with Autonomic neuropathy
Patients with urinary catheter in situ
Patients with Vascular pathology
Patient on Anticoagulant
Patients with Scoliosis
Patients with history of Spinal surgeries
Pregnancy
Severe obese patient (BMI >35Kg/m2)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of Unilateral spinal anaesthesia with 6mg of 0.5% (Hyperbaric) bupivacaine and 90mcg of buprenorphin. <br/ ><br>Timepoint: 20 minutes after spinal anaesthesia <br/ ><br>
- Secondary Outcome Measures
Name Time Method To monitor fluctuation in cardiovascular parameters (Blood Pressure, Heart Rate) before and after block, Monitor post-operative micturition time, Notice episode of post-operative nausea and vomiting, Requirement of Atropine and ephedrine intra-operatively. <br/ ><br>Timepoint: To monitor cardiovascular parameters after 20 mins of spinal anaesthesia, <br/ ><br>Monitoring 1st episode of micturition time, Monitoring first episodes of nausea and vomiting post operatively.