Lung valve registry shows promise for emphysema patients
NCT ID NCT04517916
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed French registry tracked 155 adults with severe emphysema or COPD who received Zephyr Valves, tiny devices placed in the lungs to help them work better. The goal was to see if the treatment safely improves breathing over 12 months. Researchers measured lung function and used CT scans to check for lung volume reduction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Zephyr Valve (a device placed in the lungs to reduce air trapping)
- What this could lead to
- If results are positive, this could support continued use of the Zephyr Valve as a safe and effective treatment for severe emphysema/COPD.
- What could go wrong
- This is an observational registry, not a controlled trial, so it cannot prove cause and effect. Results may not apply to all patients, and risks like infection or valve movement exist.
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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155 people
The number who actually took part.
- Started
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Jan 2021
- Finished
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Jan 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This is an all-comers Registry. Physicians at participating study centers will invite consecutive patients who are prescribed Zephyr Valve treatment to participate in the Registry and allow data collection.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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.
Inclusion Criteria: * Patients with emphysema (COPD Grade III and Grade IV) considered appropriate for the bronchoscopic lung volume reduction procedure by the physician. * Subjects who signed an Informed Consent Form to allow data collection. Exclusion Criteria: * Subjects determined to have collateral ventilation between the target(s) and ipsilateral lobe(s).
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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
Locations
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Hôpital Arnaud de Villeneuve
Montpellier, France
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Hôpital Bichat
Paris, France
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Hôpital Calmette
Lille, France
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Hôpital Charles Nicolle
Rouen, France
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Hôpital Cochin
Paris, France
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Hôpital Dupuytren
Limoges, France
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Hôpital François Mitterrand
Dijon, France
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Hôpital La Cavale Blanche
Brest, France
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Hôpital Larrey
Toulouse, France
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Hôpital Nord
Latronche, France
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Hôpital Nord
Saint-Etienne, France
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Nouvel Hôpital Civil
Strasbourg, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a heart drug combo help COPD lungs?
- Surgery-Plus-Valve combo aims to boost lung function in emphysema patients
- Surgical fix offers new hope for failed emphysema treatment
- New lung implant aims to release trapped air in emphysema patients
- New lung implant aims to ease breathing for emphysema patients