A National Registry on Chinese Patients With Cystic Fibrosis

Chinese Academy of Medical Sciences & Peking Union Medical College

Status: Enrolling

Conditions: Pulmonary Function

Study type: Observational

Funder types: Other

Identifiers

NCT05289245

XT 02

Details and patient eligibility

About

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.

Enrollment: 200 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

Fulfilled WHO clinical diagnostic criteria for CF; Was in a stable phase with no respiratory infections for nearly 4 weeks; Subjects (or their guardians) signed informed consent.

Exclusion criteria

Patients with other bronchiectasis who did not meet the inclusion criteria; Those with severe cardiac or renal disease