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Clinical Trials/CTRI/2023/10/058580
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

Sponsor
Department of Anaesthesiology

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