Status:

COMPLETED

Effects of Comprehensive Care for Knee OA

Lead Sponsor:

Indiana University

Collaborating Sponsors:

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Conditions:

Osteoarthritis

Eligibility:

All Genders

40+ years

Phase:

PHASE2

Brief Summary

We will study 300 people with knee osteoarthritis (OA) who receive their medical care from a large health maintenance organization (HMO) in Indianapolis. Our study will evaluate a comprehensive plan f...

Detailed Description

Anticipating trends toward generalism in medicine, the rheumatology community has begun to set forth guidelines for managing osteoarthritis (OA). These guidelines emphasize a comprehensive approach to...

Eligibility Criteria

Inclusion Criteria:

  • Study participants must be treated for chronic knee pain by a primary care physician at a participating HMO and satisfy American College of Rheumatology Clinical Criteria for the diagnosis of knee OA.
  • All subjects will be able to read and write English, have a telephone, and give informed consent.

Exclusion Criteria:

  • Significant hematologic, renal, hepatic, or cardiovascular disease (but not including mild/moderate hypertension) or any other serious medical condition that might preclude the subject's ability to participate fully in the project, keep clinic appointments, etc.
  • Conditions other than knee OA which limit lower extremity function and mobility and/or would confound the evaluation of knee pain and function (e.g., clinically significant spinal or hip arthritis, painful or dysfunctional feet, peripheral vascular disease, lumbar radiculopathy, stroke, etc.).
  • A known "secondary" cause of OA, including acute or chronic infectious arthritis; crystal-induced arthritis; systemic inflammatory connective tissue disease (e.g., rheumatoid arthritis, systemic lupus erythematosus); osteonecrosis; Paget's disease; or metabolic diseases, such as hemochromatosis, Wilson's disease, or ochronosis.

Key Trial Info

Start Date :

April 1 1997

Trial Type :

INTERVENTIONAL

End Date :

March 1 2001

Estimated Enrollment :

300 Patients enrolled

Trial Details

Trial ID

NCT00000404

Start Date

April 1 1997

End Date

March 1 2001

Last Update

April 30 2013

Active Locations (1)

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1

Long Hospital, Room 545

Indianapolis, Indiana, United States, 46202-5103