Comparison of two drugs for quality of block in spinal anaesthesia
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/08/044717
- Lead Sponsor
- IVY hospital mohali
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
ASA grade I and II posted for total knee arthroplasty under spinal anaesthesia
Exclusion Criteria
1. ASA grade III and IV with severe systemic illness
2. Pregnancy
3. Patient with history of heart conduction abnormalities
4. Patient on alpha blockers
5. Any known hypersensitivity to the study drugs
6. Any contraindications to SA such as local infection, coagulopathy.
7. Patient with neurologic disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method duration and quality of sensory-motor block in spinal anaesthesia and duration of postoperative analgesiaTimepoint: duration of motor anaesthesia (time taken to reach Bromage 0 from Bromage III after administration of subarachnoid block) and time of first rescue analgesia (the first time patient complains of pain at surgical site after administration of subarachnoid block)
- Secondary Outcome Measures
Name Time Method Effect on hemodynamics plus <br/ ><br>any intraoperative and/or postoperative complications <br/ ><br>Timepoint: throughout the intraoperative period, at baseline, 0 min, 2, 4, 6, 8, 10, 15, 20, 25, 30, 45, 60, 90, 120, 150, 180 mins after administration of subarachnoid block