Clin2
NCT03528525Possibly a fitRecruiting

Study of breathing-related rare genetic diseases in Chinese children

Monogenic Diseases

Part of Genetic & congenital, Lungs & breathing clinical trials.

This registry study collects and stores samples from children with breathing-related rare genetic (inherited) diseases to learn more over time. It may help researchers better understand these conditions and improve future care, especially through long-term follow-up.

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

Phase
N/A
Enrollment
200 people
Ages
1 month to 18 years
Study type
Observational

Who can take part

  • You are caring for a child (0 to 18 years old), boy or girl
  • The child has symptoms that fit a breathing-related rare genetic disease
  • You can share complete medical records (so the team can confirm the diagnosis process)
  • You agree to let the study keep and store samples in a research sample bank
  • You can and will cooperate with long-term follow-up visits or check-ins
  • A parent/guardian understands the study and agrees by signing consent

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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