CTRI/2023/10/058580
Not yet recruiting
Phase 1
Study of Transdermal Buprenorphine patch versus oral Etoricoxib for post operative pain management after total knee arthroplasty: A Randomised comparative, an open label study - Nil
Department of Anaesthesiology0 sites0 target enrollmentStarted: TBDLast updated:
Overview
- Phase
- Phase 1
- Status
- Not yet recruiting
- Sponsor
- Department of Anaesthesiology
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Patients with either sex, ASA 1,2 and 3 ,age 18 to 70 years having diagnosis of knee osteoarthritis undergoing elective unilateral total knee arthroplasty
- •Patients giving written informed consent will be taken
Exclusion Criteria
- •Patient not giving consent
- •Pregnant women
- •Lactating women
- •Contraindications for spinal anaesthesia
- •Patient with medical history of cardiopulmonary diseases, cerebrovascular diseases, liver and renal dysfunctions
- •Opioid\-dependent and opioid sensitive patients, Patients with psychiatric illness and on medication
- •Haemodynamically unstable and morbidly obese patients
- •Case of spinal anaesthesia getting converted into general anaeshesia due to intraoperative complications
Investigators
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