Registry study for cystic fibrosis in Chinese children
Part of Digestive system, Genetic & congenital, Lungs & breathing clinical trials.
This study is a registry that collects health information (and some lab samples) from Chinese children who may have cystic fibrosis (CF). It helps researchers better understand CF in children and how it is diagnosed.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Be between 0 and 18 years old
- Have symptoms that could fit cystic fibrosis (like long-term lung/sinus issues or stomach/growth problems), or have a sibling with CF
- Have test results that support CF or possible CF (based on sweat chloride results and/or CF gene changes)
- Have a legal guardian who understands the study and agrees in writing
- Be willing to let the study team collect and send the required medical specimens to the study site
- Have access to complete medical records so the team can work through the diagnosis
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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