Study of effectiveness of dexmedetomidine, when added to bupivacaine in spinal anaesthesia for lower limb surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/01/039100
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age 18 to 65 years
2.Both genders
3.ASA grade I and II
Exclusion Criteria
1.History of spine surgery, hepatic failure, neuromuscular disorders 2.chronic history of headache, backache and infection in back 3.Any absolute or relative contraindication to study drug
4.Uncooperative patients 5.Coagulopathy 6.Patient with history of cardiac or respiratory diseases
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method motor block regression in bromage score,sensory block regression by pin prick sensationTimepoint: 6 to 8 hours after intrathecal injection
- Secondary Outcome Measures
Name Time Method Onset of Sensory and motor block, Hemodynamic alterations, <br/ ><br>Numeric Rating Scale 6 hours after surgery.Timepoint: 0 min,5 min,10 min,15 min, <br/ ><br>20 min,25 min,30 min,45 min, <br/ ><br>60 min,75 min,90 min,105 min, <br/ ><br>120 min,240 min,360 min.