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Study identifier: NCT07715617 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Development of a Prediction Score for the Occurrence of Death or Lung Transplantation in Patients With Emphysema Secondary to Alpha-1-anti-tripsin Deficiency

Condition: Alpha-1-antitrypsin Deficiency · Emphysema · Artificial Intelligence (AI)  ·  Sponsor: University Hospital, Bordeaux

PhaseN/A
Planned participants230
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Emphysema linked to alpha-1-antitrypsin deficiency (DAAT): towards a better prediction of risks Emphysema caused by alpha-1-antitrypsin deficiency (DAAT) is a rare genetic disorder that can lead to serious complications, such as the need for a lung transplant or death, affecting up to 15% of patients. The only specific treatment available is a weekly infusion of alpha-1-antitrypsin (IV-AAT), an expensive and burdensome therapy. Currently, there is no reliable model to predict the course of the disease in these patients. Our study, conducted in several French hospitals, aims to develop a prediction tool combining clinical, biological, functional data and advanced medical image analysis (lung CT). This model will make it possible to identify the most at-risk patients, in order to better adapt their care, anticipate transplant needs and avoid unnecessary treatments for low-risk patients. Ultimately, this approach could also improve access to care for patients who need it most, while optimizing health system resources.

This description comes directly from the study's public registry record.

Talk to the study team

Maéva ZYSMAN, MD, PhD  ·  +335 57 65 63 38  ·  maeva.zysma@chu-bordeaux.fr

Margot GENAUD  ·  +335 25 35 21 94  ·  margot.genaud@chu-bordeaux.fr

Always discuss trial participation with your own doctor first.

Locations (4)

Hospices Civils de LyonBron, FranceRecruiting
CHU de LilleLille, FranceRecruiting
Hôpital BICHAT CLAUDE-BERNARDParis, FranceRecruiting
Bordeaux University HospitalPessac, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07715617