comparison of two types of local anaesthetics intrathecally in ambulatory elective surgery.
Phase 4
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/03/023710
- Lead Sponsor
- Department of Anaesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
60 patients of age group 18-60 years posted for infraumblical ambulatory elective surgery of45-60 minutesduration underspinal anaesthesia.
Exclusion Criteria
patients with contradictions to spinal anaesthesia,cardiac or renal insufficiency,allergic to local anaesthetics or para-aminobenzoic acid, on oral anticoagulant therapy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time to eligibility for discharge,time for complete regression of sensory and motor blockade,time to ambulation and micturitionTimepoint: Time to eligibility for discharge,time for complete regression of sensory and motor blockade,time to ambulation and micturition
- Secondary Outcome Measures
Name Time Method incidence of hypotension,bradycardia,pain requiring analgesia,postoperative nausea and vomitingTimepoint: single