KUCE: The Knee Usual Care Evaluation Study

Sponsor
Hospital for Special Surgery, New York (Other)
Overall Status
Terminated
CT.gov ID
NCT01905358
Collaborator
(none)
906
1
8.6
104.9

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Specific Aims:
    • To ascertain the long term success of non-surgical interventions intended to alleviate symptoms or slow progression of osteoarthritis of the knee.

    • To ascertain if non-operative interventions for knee osteoarthritis improve patient pain, function, and quality of life.

    • To ascertain if non-operative interventions for knee osteoarthritis affect the breakdown of articular cartilage and slow progression of osteoarthritis as evidenced by MRI or joint space narrowing on standing knee films?

    • To ascertain the amount of time between the initial entry into care at HSS and the end point of total or partial knee replacement for patients with knee osteoarthritis of varying severity.

    • To ascertain if non-operative interventions for knee osteoarthritis prolong time to knee replacement surgery.

    • To implement at electronic data capture system (EDC) for osteoarthritis patients which will store validated patient reported outcomes, physical findings, and imaging results.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    906 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official 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
    Study Start Date :
    Jul 1, 2013
    Actual Primary Completion Date :
    Mar 21, 2014
    Actual Study Completion Date :
    Mar 21, 2014

    Outcome Measures

    Primary Outcome Measures

    1. Short Form (12) Health Survey (SF-12) [6 months, 12 months, 24 months, 36 months, 48 months and 60 months.]

      Change is being assessed.

    Secondary Outcome Measures

    1. Knee injury and Osteoarthritis Outcome Score (KOOS) [6 months, 12 months, 24 months, 36 months, 48 months and 60 months.]

      Change is being assessed.

    Other Outcome Measures

    1. Whole-Organ MRI Scoring (WORMS) [baseline, 1 year, 2 years, 5 years]

      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.

    2. X-ray with Kellgren-Lawrence Grading [baseline, 4 years]

      Change is being assessed.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital for Special Surgery New York New York United States 10021

    Sponsors and Collaborators

    • Hospital for Special Surgery, New York

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Hospital for Special Surgery, New York
    ClinicalTrials.gov Identifier:
    NCT01905358
    Other Study ID Numbers:
    • 29031
    First Posted:
    Jul 23, 2013
    Last Update Posted:
    Dec 2, 2017
    Last Verified:
    Nov 1, 2017
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 2, 2017