Knee Osteoarthritis Clinical Trial
— KUCEOfficial title:
Title: The Study of Intra-articular Interventions of Platelet Rich Plasma or Hyaluronic Acid Compounds vs. Usual Care (Exercise/Diet/Supplements) in the Medical Management of Knee OA- Effects on Pain and Function; Effects on Articular Cartilage; Effects on Time to Partial or Total Knee Arthroplasty: The Knee Usual Care Evaluation (KUCE) Study
Verified date | November 2017 |
Source | Hospital for Special Surgery, New York |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The purpose of this prospective data collection is to track patients who are treated at HSS
who are confirmed with knee osteoarthritis. The registry will collect prospective patient
related and functional outcomes (including use of assistive devices), medication use and
imaging data on patients with confirmed osteoarthritis, and the effect of different medical
interventions that include PRP, Synvisc / Orthovisc /Euflexxa, bracing, suggested exercises,
supplements, and diet. Information from the data collection will be used to compare outcomes
of non-surgical alternatives with the end point being knee arthroplasty. The information
results will enhance our knowledge of the long-term efficacy and effectiveness of
non-surgical interventions intended to treat the progression of osteoarthritis.
Hypotheses:
- Different non-surgical interventions such as PRP, Synvisc®, Orthrovisc®, Euflexxa,
bracing, physical therapy, and a prescribed combination of exercise, diet, and
supplements will demonstrate statistically significant differences in patient pain and
functional outcomes compared to usual interventions including use of NSAIDs,
corticosteroid injections, and use of assistive devices such as canes.
- Non-operative interventions for knee osteoarthritis will be associated with different
rates of breakdown of articular cartilage and different rates of progression of
osteoarthritis as evidenced by MRI or joint space narrowing on standing knee films?
- Education about available non-operative treatment methods may change time the end point
of total or partial knee replacement for patients with knee osteoarthritis of varying
severity.
- Different non-operative interventions will be associated with different times to total
or partial knee arthroplasty in patient with knee osteoarthritis of similar severity.
- An electronic data capture system (EDC) for osteoarthritis patients will improve patient
care and patient outcomes.
Status | Terminated |
Enrollment | 906 |
Est. completion date | March 21, 2014 |
Est. primary completion date | March 21, 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Age greater than 30 years and less than 80 years - Knee pain for at least 6 weeks - Pain rate greater than or equal to 4/10 on a visual analog scale - Morning stiffness less than 30 minutes - Crepitus on active motion of the knee, bony tenderness, or bony enlargement of the knee - Willing and able to consider all medical treatment options used to manage osteoarthritis of the knee - No contraindications to knee radiographs or MRI - Willing to participate in a registry - Able to understand and sign a consent - Able to answer registry questions independently Exclusion Criteria: - Diagnosis of a systemic rheumatic disease or crystalline arthritis (ie RA, SLE, systemic sclerosis, psoriatic arthritis or psoriasis, gout, pseudogout, lyme arthritis, reactive arthritis, viral arthritis - pregnant or nursing - unable to give informed consent - contraindication to MRI such as indwelling paemaker or cochlear implant - requirement of metal equipment (such as oxygen) - known claustrophobia - gadolinium allergy - lack of fluency in English. Unfortunately, we do not have the financial resources to offer full translation services |
Country | Name | City | State |
---|---|---|---|
United States | Hospital for Special Surgery | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Hospital for Special Surgery, New York |
United States,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Whole-Organ MRI Scoring (WORMS) | Changes in MRI will be measured by a chance in the Whole-Organ MRI Scoring (WORMS) score of femur and tibia, and Outerbridge score for cartilage. The Boston Osteoarthritis Knee Study defined cartilage loss using the WORMS score as "an increase in the score at any sub-region compared to baseline in any of the 14 subregions of the knee scored for cartilage in each knee." For patients who have only standing radiographs available a 0.7 mm loss of joint space will be considered a significant loss over 3 years. Bruyere et al predicted that "the cut off for minimum JSN maximizing sensitivity and specificity for predicting future surgery was a change of 0.7 mm or more in minimum joint space width over a period of three years." Note: change is being assessed. | baseline, 1 year, 2 years, 5 years | |
Other | X-ray with Kellgren-Lawrence Grading | Change is being assessed. | baseline, 4 years | |
Primary | Short Form (12) Health Survey (SF-12) | Change is being assessed. | 6 months, 12 months, 24 months, 36 months, 48 months and 60 months. | |
Secondary | Knee injury and Osteoarthritis Outcome Score (KOOS) | Change is being assessed. | 6 months, 12 months, 24 months, 36 months, 48 months and 60 months. |
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