Clinical Trial Details


Research Study Summary

CRPS Treatment Evaluation 1 Study A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects with Complex Regional Pain Syndrome Type I (CRPS-I)


Subjects with Complex Regional Pain Syndrome Type I (CRPS-I)

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CW ID: 218099
Date Last Changed: August 25, 2016

Clinical Trial Snapshot

Both Male and Female
18 and up
Overall Status
24 Weeks
Facility Type


Eligibility Criteria:

Has been diagnosed with CRPS-I within 6 months of the time of Screening.
Has a history of a traumatic event inciting CRPS symptoms (eg, fracture, crushing injury, orthopedic surgery) within 12 months of Screening.
If receiving treatments or follow-up for CRPS-I, has been on a stable regime, except for chronic opioid therapy, for at least 3 weeks.

More Info

Treatment of pain associated with complex regional pain syndrome


Jay Dobson, Recruitment Coordinator
Northwest Clinical Research Center
1951 152nd Pl NE Suite 200
Bellevue, WA 98007
Phone: 425-453-0404
Fax: 425-453-1033

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Research Center Information:

Northwest Clinical Research Center

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