Low Dose Naltrexone for Chronic Pain in Osteoarthritis and Inflammatory Arthritis

Withdrawn before enrolling · Phase 2 · Has a placebo group

Conditions studied: Osteoarthritis, Arthritis, Rheumatoid, Arthritis, Psoriatic

In brief

Over 100 million Americans report chronic pain. One of the most common causes of chronic pain is osteoarthritis (OA). OA is attributable to "wear and tear," but reasons for pain are complex. Inflammatory arthritis (IA) includes multiple severe diseases that affect 2-3% of persons and require treatment with immune-suppressive drugs to prevent joint destruction. Pain often persists despite effective treatment. Pain in arthritis results from multiple sources: inflammation, perception of pain in the joint, and interpretation of pain by the brain. Unfortunately, management of pain in arthritis remains a challenge. Low dose naltrexone is a widely used but unproven "alternative" approach to chronic pain. It is attractive for study because it is safe and is proposed to work on all three pathways that contribute to pain. A small but high-quality clinical trial is needed to determine whether to invest in definitive studies.

Key facts

Study ID

NCT04115020

Run by

Brigham and Women's Hospital

People needed

0

Starts

2020-01-01

Expected to finish

2020-01-07

Last updated by the study team

2020-01-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• One or more of the following chronic conditions: osteoarthritis, rheumatoid arthritis, or non-axial spondyloarthritis
• Average daily pain interference with function (average of the 7 parts of question 9 on the Brief Pain Inventory) rated at least 4 on a scale of 0-10, and no higher than 9
• No change in medication in the past 8 weeks made with the expectation of improving pain
• No plan to start another medication or a non-pharmacologic treatment regimen likely to affect pain during the next 16 weeks
• Age at least 18
• Capable of informed consent, and willingness to comply with study procedures, including receipt of weekly phone calls from the study coordinator

You may not qualify if…

• Use of opioids including tramadol, in the past 7 days
• Pregnant, breast feeding, or unwilling to engage in contraceptive practices if sexually active and capable of conceiving
• Schizophrenia, bipolar disorder, or poorly controlled depression or anxiety
• Previous use of low-dose naltrexone for more than 8 weeks or in the past 2 weeks
• Back pain described by the patient as greater in severity than arthritic pain in all peripheral locations
• Significant kidney disease, defined as glomerular filtration rate < 30 ml/min
• Liver cirrhosis. There is no specific screening procedure to exclude cirrhosis.
• Peripheral neuropathy described by the patient as greater in severity than arthritic pain. There is no specific screening procedure.
• Plan to have surgery during the next 16 weeks
• Other qualitative circumstances that the investigator feels would make the patient a poor candidate for this clinical trial, such as an unstable social situation or unreliable transportation

Where it is running

• Brigham and Women's Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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