Czech Alpha-1 Antitrypsin Deficiency Registry, the National Observational Study.
Status: Recruiting
Study Type: Observational
SUMMARY
Alpha-1-antitrypsin deficiency is the most common congenital disease of the respiratory system, leading to early pulmonary emphysema or bronchiectasis. Pulmonary involvement significantly accelerates active cigarette smoking. Patients with alpha-1-antitrypsin deficiency may also have liver cirrhosis, vasculitis, skin or intestinal disorders. The AATD Registry is a non-interventional multicenter retrospective prospective longitudinal follow-up of patients with alpha-1-antitrypsin deficiency. The aim of the AATD National Registry is to collect and analyze clinical data in patients with alpha-1 antitrypsin deficiency.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:
• Patients with alpha-1-antitrypsin deficiency
Contact Information
Primary
Katerina Kusalova, Ing
kusalova@biostatistika.cz
+420723949465
Time Frame
Start Date: 2018-01-01
Estimated Completion Date: 2035-12-31
Participants
Target number of participants: 300
Related Therapeutic Areas
Sponsors
Collaborators: Masaryk University
Leads: Thomayer University Hospital