Comparative study of two different drugs when used with a standard drug ,in patients undergoing spinal anaesthesia to find out which has better patient tolerence and pain releif in orthopaedic surgeries
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/05/052583
- Lead Sponsor
- College of Medicine and JNM hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a)Patient who gives written consent.
b)ASA-Ð? &Ð?Ð?
c)Age â?? 18-55 years of both sexes
d)Any patient posted for elective lower extrimity orthopedic surgery to be done under subarachnoid block
Exclusion Criteria
a)Patient who does not give or not in a mental state to consent due to any reason.
b)Any contraindication to SAB
c)Patient requiring intraoperative any general anaesthetic aid
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of analgesic duration following, hyperbaric Ropivacaine-Fentanyl vs Bupivacaine- fentanyl :duration of sensory, motor block, spinal anaesthesia, time of rescue analgesiaTimepoint: Comparison of analgesic duration following, hyperbaric Ropivacaine-Fentanyl vs Bupivacaine- fentanyl at 15, 30,45,60
- Secondary Outcome Measures
Name Time Method Comparison of postoperative pain relief following, Ropivacaine-Fentanyl vs Bupivacaine-fentanylTimepoint: Continuous ECG in lead II, SBP, DBP, MAP, HR, RR, SpO2 will be recorded 15 minutes before and at the time of spinal anaesthesia, then at 1 minute, at 3 minute, at 5 minute, thereafter at 5 minutes interval throughoutthe entire surgical procedure and at 15 minutes interval during first 60 minutes of post-operative period.