To compare the advantage and disadvantage of using bupivacaine 0.5% heavy, isobaric levo-bupivacaine 0.5% and hyperbaric ropivacaine 0.75% in spinal anaesthesia during brachytherapy procedure
Phase 4
Completed
- Conditions
- Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
- Registration Number
- CTRI/2023/07/054588
- Lead Sponsor
- AIIMS NEW DELHI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Patients undergoing interventional brachytherapy procedures under sole spinal anaesthesia.
Exclusion Criteria
patient refusal, allergic to study drugs, contraindication for neuraxial anasthesia, emergency surgeries.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of sensory and motor blocksTimepoint: baseline (before any intervention), and intraoperatively every 2 min till adequate surgical anaesthesia achieved after IT drug administration, followed by every 10 mins after completion of surgery
- Secondary Outcome Measures
Name Time Method Onset of sensory and motor block, VAS score, MAP and HRTimepoint: same as primary outcome