It is to compare hyperbaric Ropivacaine with hyperbaric bupivacaine for spinal anaesthesia in patients undergoing prostate resection surgeries
Not Applicable
Completed
- Conditions
- Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
- Registration Number
- CTRI/2023/08/056816
- Lead Sponsor
- Dept. of Anaesthesiology and Critical Care.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Adult male patients belonging to ASA grade I-III of age less than or equal to 65 years undergoing transurethral resection of prostate under spinal anaesthesia
Exclusion Criteria
Contraindications to spinal anaesthesia
Refusal to give consent
History of allergy or hypersensitivity to local anaesthetics
Body mass index more than 30kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the total duration of sensory block in both the groups.Timepoint: Sensory block will be assessed by pinprick for pain along the mid-line. The sensory block will be assessed every two minutes for the initial 10 minutes, every five minutes for the next 30 minutes and thereafter at the interval of 15 minutes till 2 segment regression (defined as recovery of sensory block two segments from the highest level achieved in that patient).
- Secondary Outcome Measures
Name Time Method Onset, highest level attained and regression of motor block.Timepoint: Motor block will be assessed every two minutes for the initial 10 minutes, every five minutes for the next 30 minutes and thereafter at the interval of 15 minutes till complete regression of motor block to grade 1.