Actively Recruiting

Phase 4
Age: 21Years +
All Genders
NCT05336968

Triamcinolone Ketorolac (TriKe) Knee Trial

Led by United Health Services Hospitals, Inc. · Updated on 2024-05-08

150

Participants Needed

1

Research Sites

171 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cortisone injections are commonly used in the treatment of osteoarthrosis of the knee, but there are known detriments to cortisone including localized tissue atrophy near the injection site and acceleration of joint degeneration, as well as contraindications, such as uncontrolled diabetes. Ketorolac is a non-steroidal anti-inflammatory with decades of clinical data that is most commonly injected intramuscularly. There is rising interest in using ketorolac as an intra-articular injectant substitute or adjunctive to cortisone. This may potentially improve clinical outcomes or decrease adverse effects. Although intra-articular use of ketorolac is increasing in orthopedics and sports medicine, there is limited data in the literature comparing these two injectants in prospective, randomized trials, and no data that evaluates combining the two injectants. Primary objectives are to evaluate the efficacy of intra-articular ketorolac compared to cortisone on knee osteoarthrosis and to evaluate whether the combination of ketorolac and cortisone is superior to either alone.

CONDITIONS

Official Title

Triamcinolone Ketorolac (TriKe) Knee Trial

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Knee pain with diagnosis of osteoarthritis or osteoarthrosis
  • Weight-bearing x-rays within the last year adequate to assess Kellgran-Lawrence OA stage
  • Age above 21 years
  • Sufficient English proficiency to complete surveys
  • Willingness to complete follow-up surveys
Not Eligible

You will not qualify if you...

  • Prior knee injection in the last 3 months
  • Knee surgery within the last year
  • Contraindications to cortisone, ketorolac, or local anesthetic
  • Uncontrolled diabetes
  • Systemic steroid use in the last 3 months
  • Body mass index greater than 50
  • Non-ambulatory status
  • Known kidney disease
  • Current opioid use

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

United Health Services Sports Medicine Department

Vestal, New York, United States, 13850

Actively Recruiting

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Research Team

T

Terri Peters, RN MSN CCRP

CONTACT

B

Benjamin Kammerman, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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