Actively Recruiting

Phase 4
Age: 18Years - 80Years
All Genders
NCT06269770

Tapentadol vs Tramadol in Total Knee Arthroplasty

Led by University of Thessaly · Updated on 2024-05-14

96

Participants Needed

1

Research Sites

108 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Compare the effectiveness of tapentadol and tramadol as part of a multimodal analgesia treatment for Total Knee Replacement (TKR).

CONDITIONS

Official Title

Tapentadol vs Tramadol in Total Knee Arthroplasty

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for elective Total Knee Replacement
  • ASA Physical Status classification I to III
Not Eligible

You will not qualify if you...

  • Patient refusal to participate
  • Cognitive dysfunction
  • Severe psychiatric disease
  • Current use of MAO inhibitors, tricyclic antidepressants, or serotonin reuptake inhibitors
  • Inability to speak Greek
  • Known allergy to tapentadol or tramadol
  • Contraindications to any study drugs
  • Chronic renal failure with GFR below 50 ml/h
  • Liver failure
  • Regular or misuse of opioids
  • Pregnancy
  • Patients receiving general anesthesia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Of Larissa

Larissa, Thessaly, Greece, 41110

Actively Recruiting

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Research Team

E

Eleni Arnaoutoglou, MD, PhD

CONTACT

M

Metaxia Bareka, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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