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Clinical Trial Summary

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 attend either in-person or virtual study visits and complete questionnaires.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02502162
Study type Interventional
Source Stanford University
Contact Birute Gedrimaite
Phone (650) 497-0485
Email birute@stanford.edu
Status Recruiting
Phase N/A
Start date June 2015
Completion date June 2025

See also
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