Actively Recruiting

Phase 1
Age: 18Years +
All Genders
Healthy Volunteers
NCT05906433

Optimal Anesthetic for Corticosteroid Injections for Knee Osteoarthritis

Led by Foundation for Orthopaedic Research and Education · Updated on 2024-12-09

75

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

Sponsors

F

Foundation for Orthopaedic Research and Education

Lead Sponsor

F

Florida Orthopaedic Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

To evaluate pain relief from corticosteroid injection with and without anesthetic as well as with variable volume of anesthetic. Pain relief will be measured using the VAS pain score at the time of the injection as well as several time points following the injection to capture pain relief longevity. The investigators intend to evaluate how well the patients tolerate corticosteroid mixtures without anesthetic as well as with different volumes of anesthetic. Primary measure will be the time from procedure when postoperative status is considered success (as measured by global perceived improvement score).

CONDITIONS

Official Title

Optimal Anesthetic for Corticosteroid Injections for Knee Osteoarthritis

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients must be 18 years of age or older and able to consent for themselves.
  • Diagnosis of primary osteoarthritis.
  • Osteoarthritis grade Kellgren Lawrence Stage II or III.
Not Eligible

You will not qualify if you...

  • Patients with other forms of arthritis such as inflammatory arthritis.
  • History of narcotic use within the past 6 months.
  • Osteoarthritis grade Kellgren Lawrence Stage I or IV.
  • Pregnant women.
  • Prisoners.

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

Florida Orthopaedic Institute

Tampa, Florida, United States, 33637

Actively Recruiting

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Research Team

A

Anne Meredith Baldy, CCRC

CONTACT

D

Debbi Warren, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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