To evaluate and compare the efficacy of intravenous antagonists in preventing shivering during elective LSCS under subarachnoid block.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064015
- Lead Sponsor
- Dr Ashwini R
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
•Parturients willing to give informed and written consent
•ASA physical status II
•Parturients with Body Mass Index 20 – 30 Kg / M2
•Elective LSCS with singleton pregnancy
Exclusion Criteria
1.Parturients with known hypersensitivity to the study drugs
2.Parturients who have received the study drugs 24 hours before the surgery.
3.Parturients with emetic episodes 24 hours prior to the surgery
4.Parturients who are on opioids, who require sedation, intraoperative blood transfusion.
5.Parturients with pre operative temperature = 38 ? C or = 36.6 ? C
6.Parturients having Parkinson’s disease or movement disorders or seizures.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perioperative shiveringTimepoint: 5 mins, 10 mins, 15 mins, 20 mins, 25 mins, 30 mins followed by every 30 minutes till return of modified bromate scale of 6
- Secondary Outcome Measures
Name Time Method Vitals AssessmentTimepoint: 0 mins, 30 mins, 60 mins, 2 hours