Comparing Dexmedetomidine and Fentanyl with Ropivacaine for spinal anaesthesia
Phase 4
- Conditions
- Health Condition 1: M849- Disorder of continuity of bone, unspecifiedHealth Condition 2: 7- OsteopathicHealth Condition 3: M848- Other disorders of continuity of bone
- Registration Number
- CTRI/2023/09/058000
- Lead Sponsor
- Rajendra institute of medical sciences Ranchi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.patients consent
2.ASA physical class 1 and 2
3.elective lower limb orthopaedic surgery cases with duration of surgery not more than 2 hours
Exclusion Criteria
1.patient having contraindication for spinal anesthesia
2.pregnant females
3.patient with chronic disease
4.patient with BMI >30kg/m2
4.patient shorter than 150cms
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset and duration of sensory block in all three groupsTimepoint: From time of induction till T10 level of block achieved for onset(within 30 mins of induction). <br/ ><br>For duration,from time of induction till patient feels the sensation at S1 dermatome <br/ ><br>(till 12hrs after induction)
- Secondary Outcome Measures
Name Time Method maximum sensory blockade attained & time taken for sameTimepoint: 30 -45 mins after induction;onset & duration of motor blockTimepoint: 30mins post induction for onset <br/ ><br>12hrs post induction for duration;quality of motor block & time taken for the maximum motor blockadeTimepoint: till 30 mins post induction;time taken for two segment sensory regressionTimepoint: till 12 hrs post induction;total duration of analgesiaTimepoint: till 12hrspost induction