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Enrolling by invitation Observational

Thrombotic RIsk FActors in AL-goneurodystrophy

NCT07435207 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-01-26
Last updated
2026-02-27

Condition(s) studied

Algoneurodystrophy

Study summary

The primary objective of the study is to evaluate the prevalence of blood prothrombotic factors in CRPS patients and their role in predicting response to neridronic acid treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:Clinical (according to Budapest clinical diagnostic criteria for CRPS) * patients aged 18 years or more Exclusion Criteria:patients unable to give consent \-

Primary outcome measure(s)

  • Pain VAS — 1,3 and 6 months after therapy
    change in Pain VAS

Trial sites (1)

FacilityCityRegionStatus
Fondazione IRCCS Policlinico San Matteo di Pavia Pavia Pavia
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07435207 on ClinicalTrials.gov ↗ ← All trials in Italy