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Clinical Trial Summary

Cystic fibrosis (CF) is autosomal recessive, genetic disorder cause of cystic fibrosis transmembrane regulatory (CFTR) gene mutation. CF often is observed in caucasian population. CFTR protein in cell apical membrane is canal responsible of transport sodium and clorid ions. Impaired sodium ion transport causes production viscous mucus. Disease include problems such as mucus, breathlessness and coughing. Blood glucose levels fluctuation are observed. This study aims comparison between lung function, functional capacity, muscle strength, physical activity, physical fitness and activities of daily living activities in cystic fibrosis with and without abnormal glucose tolerance


Clinical Trial Description

The study aimed that comparison of clinical parameters in children with and without abnormal glucose tolerance in Cystic fibrosis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04503408
Study type Observational
Source Hacettepe University
Contact
Status Completed
Phase
Start date September 13, 2019
Completion date March 11, 2020

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