Scientists hunt for genetic clues in rare lung syndrome
NCT ID NCT02439528
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 250 people to understand why some smokers develop a rare lung condition called combined pulmonary fibrosis and emphysema (CPFE). Researchers compared telomere length and genetic mutations in patients with CPFE, those with only fibrosis or emphysema, and healthy individuals. The goal was to find genetic differences that might explain why some people get this severe disease.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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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.
Contacts and locations
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Locations
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Hôpital Albert Michallon, CHU de Grenoble
Grenoble, 38 043, France
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Hôpital Nord, CHU de Saint-Etienne
Saint-Etienne, 42055, France
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Hôpital pneumologique et cardiovasculaire Louis Pradel, HCL
Bron, 69677, France