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Study identifier: NCT05925790 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Clinical Phenotypes in Pericarditis: IL-1RA Antibodies and suPAR Levels

Condition: Pericarditis  ·  Sponsor: ASST Fatebenefratelli Sacco

PhaseN/A
Planned participants146
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

This study aims to investigate the pathophysiology of recurrent pericarditis (RP) by testing for neutralizing autoantibodies against interleukin-1 receptor antagonist (IL-1RA) and measuring soluble urokinase plasminogen activator receptor (suPAR) levels. The hypothesis is that these tests will provide insights into both the inflammatory and non-inflammatory phenotypes of RP, shedding light on the underlying mechanisms. The study will assess the correlation between antibody levels, suPAR levels, and markers of cardiac damage and inflammation. Longitudinal testing during acute episodes and intercritical phases is also planned. The results may guide the use of anakinra, an IL-1 receptor antagonist, in specific clinical scenarios and optimize treatment strategies for RP.

This description comes directly from the study's public registry record.

Talk to the study team

Maddalena A Wu  ·  +393392883379  ·  maddalena.wu@unimi.it

Always discuss trial participation with your own doctor first.

Locations (9)

Saarland UniversityHomburg, GermanyRecruiting
University Children's Hospital MuensterMünster, GermanyNot Yet Recruiting
University Hospital TübingenTübingen, GermanyNot Yet Recruiting
A.O.U. CareggiFlorence, ItalyNot Yet Recruiting
Luigi Sacco Hospital - ASST Fatebenefratelli SaccoMilan, ItalyRecruiting
Fatebenefratelli Hospital - ASST Fatebenefratelli SaccoMilan, ItalyRecruiting
Ospedale Galeazzi Sant'Ambrogio - IRCCS, Poliambulatorio Cardiovascolare Cardiologia UniversitariaMilan, ItalyNot Yet Recruiting
Policlinico di Milano Ospedale Maggiore, Fondazione IRCCS Ca' GrandaMilan, ItalyNot Yet Recruiting
Ospedale Santa Maria della Misericordia dell'ASU-FCUdine, ItalyNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT05925790