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Clinical Trial Summary

Cystic fibrosis (CF) is a rare autosomal recessive disease involving multiple organs, especially the lungs and digestive organs. It is most commonly seen in Caucasians. Only a few Chinese CF patients have been described in literature, taking into account the large population of China. The main objectives of this study are to accurately evaluate the prevalence of CF, the status of disease, the diagnosis and treatment, the quality of care, and the health related outcomes in China.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05289245
Study type Observational [Patient Registry]
Source Peking Union Medical College Hospital
Contact Xinlun Tian, M.D.
Phone 86-10-69155039
Email tianxl@pumch.cn
Status Recruiting
Phase
Start date April 1, 2022
Completion date October 1, 2032

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