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NCT07811362Possibly a fitRecruiting

Tracking long-term outcomes for CRPS after neridronate treatment

Complex Regional Pain Syndrome I (CRPS I)

Part of Brain & nervous system clinical trials.

This study is a registry that tracks people with Complex Regional Pain Syndrome (CRPS) who already received neridronate infusions in a previous trial. It looks at how they do over the long term to learn more about the treatment's lasting effects.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
270 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must have been part of the CRPS-RISE study (the earlier trial for CRPS).
  • You must have received all 4 infusions of neridronate (a drug given through an IV) or the matching placebo during that trial.
  • You must have completed the final clinic visit at about 6 weeks after the last infusion.
  • If you also took part in the open-label extension (a follow-up phase where everyone received the drug), you need to have completed the same 4 infusions and the final visit there too.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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