A Comparison of Clinical Parameters in With and Without Abnormal Glucose Tolerance. (NCT04503408) | Clinical Trial Compass
CompletedNot Applicable
A Comparison of Clinical Parameters in With and Without Abnormal Glucose Tolerance.
Turkey (Türkiye)40 participantsStarted 2019-09-13
Plain-language 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
Who can participate
Age range10 Years – 18 Years
SexALL
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Inclusion criteria
✓. Cystic fibrosis with impaired glucose tolerance or cystic fibrosis-related diabetes for Abnormal glucose tolerance group
✓. Cooperation for tests
✓. Indıviduals without an orthopedic or neurological problem and serious cardiac problems that effecting tests,
✓. To volunteer for the study.
✓. Cystic fibrosis with normal glucose tolerance
✓. Cooperation for tests
✓. Indıviduals without an orthopedic or neurological problem and serious cardiac problems that effecting tests,