Czech AATD Registry
Recruiting now
Conditions studied: Alpha-1-antitrypsin Deficiency
In brief
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.
Key facts
- Study ID
- NCT05178277
- Run by
- Thomayer University Hospital
- People needed
- 300
- Starts
- 2018-01-01
- Expected to finish
- 2035-12-31
- Last updated by the study team
- 2022-01-05
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with alpha-1-antitrypsin deficiency
You may not qualify if…
- Patient disagreement with inclusion in the study
Where it is running
- Thomayer university hospital — Prague, Czech Republic, Czechia (enrolling)
Full record on ClinicalTrials.gov
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