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Condition / disease
Location
Status: Recruiting

Czech AATD Registry

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.

Participants needed: 300
Trial details
Biological sex: AllType: ObservationalSponsor: Thomayer University HospitalUpdated: Jan 5, 2022Locations: 1Duration: 20 Years
Eligibility criteria

Patients with alpha-1-antitrypsin deficiency

Patient disagreement with inclusion in the study