Platelets in Cystic Fibrosis Lung Inflammation
NCT05339724 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 53
Last updated 2022-05-20
Summary
Cystic fibrosis (CF) is a chronic multiorgan disorder caused by mutations in the CFTR (cystic fibrosis transmembrane conductance regulator) gene. Chronic airway infection by bacterial pathogens accounts for the progressive, suppurative pulmonary disease that leads to significant morbidity and mortality in patients with CF. Neutrophil recruitment to the lungs accounts the most important contributor to pulmonary destruction. However, there is evidence that platelets may also have an important role in the pathogenesis of inflammation. To our knowledge, there is few information in platelet levels in patients with cystic fibrosis during pulmonary exacerbation, chronic airway colonization and when stable.
Conditions
- Platelet Levels and Mean Platelet Volume in Patients With CF
Interventions
- OTHER
-
platelet count and mean platelet volume are obtained from whole blood count
The records of cystic fibrosis patients will be retrospectively evaluated for acute pulmonary exacerbation, chronic airway colonization for bacteria, clinical stable status. PC and MPV will be obtained and matched in 6 groups (described above). Then, PC and MPV will be compared among the groups.
Sponsors & Collaborators
-
Mersin Training and Research Hospital
lead OTHER_GOV
Principal Investigators
-
Ali Özdemir, MD · Assoc Prof, Mersin City Research & Training Hospital
-
Murat Ersoy, MD · Clinical Pediatrician, Mersin City Research & Training Hospital
Eligibility
- Min Age
- 12 Months
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-04-08
- Primary Completion
- 2022-04-30
- Completion
- 2022-05-01
Countries
- Turkey (Türkiye)
Study Locations
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