Clin2
NCT01440218Possibly a fitEnrolling by invitation

Study for rare illnesses and treatment reactions in families

Rare DiseaseIdiopathic Disease

This trial looks for answers in rare illnesses that either have no known cause or have not improved with usual treatments. It also studies rare harmful reactions that happen after medicines, vaccines, or medical devices, and may involve family members of the affected person.

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

Phase
N/A
Enrollment
10 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a rare illness with no known cause so far, or it does not improve with standard treatments
  • The affected person had a rare harmful reaction tied to a medicine, vaccine, or device
  • You are a family member of the person with the affected illness
  • You (or your legal guardian) can give informed consent to join the study
  • You do not have serious health or mental/emotional conditions that would interfere with study participation

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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