Palo Alto, California 94304


Purpose:

The investigators are testing treatment with low-dose naltrexone (LDN) for symptom relief of complex regional pain syndrome (CRPS). Study participants will be randomly assigned to receive either LDN or placebo for a period of several weeks. During this period participants will be asked to come to several visits, which will include sensory testing, physical assessments, and questionnaires.


Criteria:

Inclusion Criteria: - Upper and/or lower extremity CRPS - On stable treatment for 3 months - CRPS for at least 1 year - Meet the Budapest criteria for CRPS at time of the study. Exclusion Criteria: - Any known allergy to naltrexone or naloxone - Use of prescription opioid analgesics or illegal opioid use - Current of planned pregnancy.


NCT ID:

NCT02502162


Primary Contact:

Principal Investigator
Sean Mackey, MD, PhD
Stanford University

Maria L Adelus
Phone: (650) 724-9320
Email: madelus@stanford.edu


Backup Contact:

N/A


Location Contact:

Palo Alto, California 94304
United States

Maria L Adelus
Phone: 408-386-2143
Email: madelus@stanford.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 23, 2017

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