Comparison of Onset, duration, quality of postoperative analgesia of epidurally administered Bupivacaine with Dexmedetomidine group and Bupivacaine with Buprenorphine group.
Not Applicable
- Conditions
- Health Condition 1: M170- Bilateral primary osteoarthritis of knee
- Registration Number
- CTRI/2023/10/058865
- Lead Sponsor
- vydehi 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)ASA 1 & 2
2)PATIENTS UNDERGOING TOTAL KNEE AND HIP REPLACEMENT SURGERIES
3)Uneventful intraoperative patients
Exclusion Criteria
1)ASA 3 & 4
2)ALLERGY TO LOCAL ANESTHETICS, DEXMEDETOMIDINE AND BUPRENORPHINE
3) BLEEDING AND NEUROMUSCULAR DISORDERS
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare onset, duration, quality of postoperative analgesia of epidurally administered bupivacaine with dexmedetomidine and bupivacaine with buorenorphineTimepoint: To compare onset, duration, quality of postoperative analgesia of epidurally administered bupivacaine with dexmedetomidine and bupivacaine with buorenorphine
- Secondary Outcome Measures
Name Time Method assess and compare the haemodynamic parameters, side effects and time for ambulationTimepoint: after giving epidural topup onset of analgesia, sedation, duration of analgesia, haemodynamic parameters, mobilization time