Clin2
NCT05364294Possibly a fitRecruiting

Molecular testing for rare inflammatory (autoinflammatory) diseases

Inflammatory DiseaseGenetic DiseaseSomatic MutationMolecular Sequence VariationMolecular Pathway Deregulation

Part of Genetic & congenital clinical trials.

This study uses lab testing to better identify the cause of certain rare inflammatory conditions that happen without infection. Finding the cause may help doctors choose more targeted care for you or your child.

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

Phase
N/A
Enrollment
300 people
Ages
1 week to 120 years
Study type
Observational

Who can take part

  • You have symptoms of inflammation without an infection being found (an “aseptic” inflammatory problem).
  • You may have fever that goes away on its own, or repeated digestive symptoms like belly pain/diarrhea.
  • You may have joint or muscle pain, or chest-related inflammation such as pericarditis (inflammation around the heart).
  • You may have skin or eye/ear symptoms (such as uveitis or hearing problems).
  • You may have kidney problems related to inflammation (for example, amyloidosis).
  • You are not under legal protections like guardianship or similar court-ordered arrangements.

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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