40
Participants
Start Date
January 2, 2024
Primary Completion Date
August 31, 2026
Study Completion Date
November 30, 2026
Low dose naltrexone
While naltrexone is FDA-approved for treatment of alcohol or opioid addition, this study will be looking at how naltrexone, when dosed very low, may reduce the painful symptoms associated with CRPS. Naltrexone is not FDA-approved for pain management treatment of CRPS at this time, and therefore the study intervention is using the drug in an off-label manner.
Placebo sugar capsules
The external appearance of the capsules prepared by the pharmacy will be identical to the LDN capsules. The inactive capsule ingredients will be microcrystalline cellulose (MCC) and Magnesium stearate
Hospital for Special Surgery, New York
Hospital for Special Surgery, New York
OTHER