A clinical trial to study the effect of intranasal dexmedetomidine on spinal anaesthesia shivering .
Not Applicable
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2024/08/071988
- Lead Sponsor
- Sri Venkateswara Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age between 20-45 years.
2.ASA-PS II and III.
3.Weight between 45 to 75 kgs.
4.Normothermic 36.5 to 37.5 degree C
5.Stable hemodynamics SBP greater than 100mmhg.
Exclusion Criteria
1.Declining to participate or receive spinal anaesthesia.
2.Absolute contraindications to spinal anaesthesia.
3.Height less than 100 cms.
4.Morbid obesity with BMI greater than 40KG/M2 .
5.Known allergy to dexmedetomidine or bupivacaine.
6.Use of epidural catheter.
7.Presence of significant cardiac, liver or renal problems.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO DETERMINE THE OCCURENCE OF CLINICALLY SIGNIFICANT POST SPINAL ANAESTHESIA SHIVERINGTimepoint: Immediately after spinal anaesthesia, 5,10,15,20,30,45,60 mins and at the end of the surgery.Post operative every 30 mins for 120 mins
- Secondary Outcome Measures
Name Time Method GRADE OF SHIVERING <br/ ><br>GRADE OF SEDATION <br/ ><br>OCCURENCE OF NAUSEA,VOMITING, <br/ ><br>BRADYCARDIA,HYPOTENSION.Timepoint: Immediately after spinal anaesthesia,post spinal at 1,3,5,10,20,30,40,50 min,1,2,4,6 hrs