Last updated on June 2018

Placebo-controlled efficacy and safety trial of intravenous neridronic acid in subjects with complex regional pain syndrome (CRPS)


Brief description of study

To demonstrate the superior efficacy of a cumulative dose of 400 mg intravenous neridronic acid versus placebo for the treatment of CRPS-related pain.

Clinical Study Identifier: TX205745

Contact Investigators or Research Sites near you

Start Over

Jim Faucett, Recruitment Coordinator

Northwest Clinical Research Center
Bellevue, WA USA
  Connect »

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


Receive Emails About New Clinical Trials!

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.