Doxycycline and OA Progression

• Status: Completed
• Trial end date: 2001-07-01
• Target enrollment: 0
• Participant gender: Female

Summary

This study will determine whether doxycycline decreases the severity or rate of progression of osteoarthritis (OA) in the knee. Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most popular agents used to treat OA, but elderly women, in whom OA is especially common, are at greatest risk of developing serious side effects from NSAIDs.

Our study targets overweight middle-aged women who have OA in one knee. Half of the 432 study participants will receive the treatment (doxycycline) and half will receive a placebo (inactive pill). Treatment with doxycycline (or placebo) will last 30 months, and participants and researchers will not know who is receiving doxycycline and who is receiving placebo until the end of the study. We will look for narrowing of the joint space in the knee that was not affected by OA at the start of the study. Joint space narrowing is a sign of OA. We will also use questionnaires to evaluate participants' symptoms and functioning.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Indiana University
• Collaborators: National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS); National Institute on Aging (NIA)
• Treatments: Doxycycline

Criteria

Inclusion Criteria:

• Women 45-64 years of age.

• Upper tertile of sex-, age- and race-adjusted norms for body mass index.

• Unilateral knee OA at baseline.

• Postmenopausal status or otherwise incapable of childbearing.

• Ability to ambulate (move about) independently without assistive devices.

• Ability to read and write in English or Spanish and give informed consent.

Exclusion Criteria:

• Premenopausal status (unless subject has had a hysterectomy).

• Current use of any investigational drug.

• 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.

• Prior surgery (including arthroscopy) of the contralateral knee.

• Significantly abnormal laboratory values at the time of enrollment.

• Pigmented villonodular synovitis of the knee.

• Synovial chondromatosis.

• Charcot arthropathy.

• A known "secondary" cause of OA, including acute or chronic infectious OA; 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. Chondrocalcinosis, however, will not be an exclusion criterion.

• 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.).

• Steroid injection into either knee within past 3 months.

• A history of photosensitivity (sensitivity to light) or any other adverse reaction to a tetracycline.

• Failure to pass a "faintness-of-heart" test (pre-randomization compliance test).

• Prior chronic use of tetracycline (e.g., for severe acne).

• Severe OA (Kellgren and Lawrence Grade IV) of the index knee.

• Salicylate use, with a mean dose >2g/d.

• Institutionalization.