AI model could predict who needs a lung transplant for rare emphysema
NCT ID NCT07715617
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This study aims to create a prediction tool for people with emphysema caused by alpha-1-antitrypsin deficiency, a rare genetic disorder. Researchers will analyze clinical data, lab results, and lung CT scans from 230 patients to identify those at highest risk of death or needing a lung transplant within five years. The goal is to help doctors personalize care and avoid unnecessary treatments for low-risk patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this prediction tool could help doctors identify which patients need a lung transplant or intensive care sooner, and spare low-risk patients from unnecessary treatments.
- What could go wrong
- The model is based on past patient data and may not work perfectly for all individuals. It is still in development and needs validation before it can be used in clinics.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 230 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Mar 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The subjects included will be any patients followed and diagnosed between 2010 and 2025 in the pulmonology department for emphysema and COPD secondary to alpha-1 antitrypsin deficiency ZZ, Znull, ZMalton, Z and rare mutations, based on the diagnosis of emphysema made from an initial thoracic CT scan (+/- 12 months after diagnosis).
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
1. Inclusion criteria: * diagnosed between 2010 and 2025 * in the pulmonology department * diagnosis of emphysema and COPD secondary to alpha-1 antitrypsin deficiency ZZ, Znull, ZMalton, Z and rare mutations, * emphysema according to the initial thoracic CT scan (+/- 12 months after diagnosis). 2. Exclusion criteria: * Age \<18 years * Patient opposed to the use of their data for research purposes * Patient deprived of liberty by judicial decision * Patient not affiliated with a social security scheme * no CT scan available * no lung function test available the year around CT scan
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Bordeaux University Hospital
RECRUITINGPessac, 33600, France
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CHU de Lille
RECRUITINGLille, 59000, France
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Hospices Civils de Lyon
RECRUITINGBron, 69677, France
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Hôpital BICHAT CLAUDE-BERNARD
RECRUITINGParis, 75018, France
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