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New lung implant could help severe emphysema patients breathe easier

NCT ID NCT07086339

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a new device called the IAB 50 Flex, an implantable artificial bronchus for adults with severe COPD or emphysema. The trial will enroll 20 participants across two hospitals to check if the implant is safe and if it helps improve breathing and daily activity. The main goal is to see if there are any serious side effects related to the device or procedure within 90 days.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
implantable pulmonary stent (IAB 50 Flex)
What this could lead to
If successful, this implant could offer a new way to help people with severe emphysema breathe easier and improve daily function.
What could go wrong
This is a very early, small trial (20 people) focused on safety, not yet proven to work. The implant may cause serious side effects or not help breathing.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 20 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2026

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

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.

Ages

22 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Signed Informed Consent 2. Diagnosis of COPD/emphysema 3. At least 22-years of age 4. 18 ≤ BMI ≤ 32 5. 6-minute walk Distance of between 100 - and 400 meters 6. Stable disease with less than 10-mg prednisone (or equivalent) daily 7. Non-smoking for 4-months prior to screening interview (this includes tobacco, vaping, marijuana, etc.). 8. FEV1 between 15% and 45% of predicted value at baseline exam 9. FEV1/FVC \<70% 10. Subject has ≥25% emphysema destruction score in each lung defined by areas of low attenuation less than -950 HU, as determined by CT core lab. 11. Subject has homogeneous or heterogeneous emphysema, and at least one lung has a 15% difference between upper and lower lobes in emphysema destruction score less than -950 HU, as determined by CT core lab. 12. RV \> 175% of predicted value. 13. mMRC score ≥ 2 Exclusion Criteria: 1. Currently participating in another clinical study that involves surgery, interventional or pharmaceutical treatment 2. α-1 Antitrypsin deficiency 3. Women of child-bearing potential 4. More than 2 COPD exacerbation episodes requiring hospitalization in the last year prior to screening 5. Any COPD exacerbations requiring hospitalization within 6-weeks of planned intervention 6. Two or more instances of pneumonia episodes requiring hospitalization in the last year prior to screening 7. Clinically significant mucus production or chronic bronchitis 8. Myocardial Infarction or unstable / uncontrolled congestive heart failure within 6-months of screening 9. Prior lung transplant, LVRS, bullectomy, lobectomy or endoscopic lung volume reduction (ELVR) 10. Clinically significant bronchiectasis 11. Unable to safely discontinue anti-coagulants or platelet activity inhibitors for 7-days 12. Uncontrolled pulmonary hypertension (systolic pulmonary arterial pressure \>45 mm Hg) or evidence or history of cor pulmonale as determined by recent echocardiogram 13. Suspected malignant pulmonary nodule or other lung cancer 14. HRCT collected per CT scanning protocol within the last 6 months of screening date and evaluated by clinical site personnel using 3D segmentation software shows: * Large bullae encompassing greater than 30% of either lung * Insufficient landmarks to evaluate the CT study using the software as it is intended * All lobes are less than 25% parenchyma diseased (\< -950 HU). 15. Any cardiac comorbidity which the PI believes would compromise the safety of the patient after an IAB implant 16. TLC \< 100% predicted at screening 17. DLCO \< 15% or \> 50% of predicted value at screening 18. PaCO2 \> 50 mm Hg at screening 19. PaO2 \< 45 mm Hg in room air at screening 20. Plasma cotinine level \> 13.7 ng/ml or carboxyhemoglobin (arterial or ear lobe capillary) \>2.5% at screening. 21. Current diagnosis of substance abuse disorder. 22. Current diagnosis of any of the following: Major Depressive Disorder (MDD), Schizoaffective Disorder, Schizophrenia, Borderline Personality Disorder, Bipolar Disorder 23. Any other conditions, which, in the opinion of the Investigator, would make the patient unsuitable for inclusion, or could interfere with the patient participating in or completing the study.

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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.

  1. The places running it

    2 sites in 2 countries. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • DUPUYTREN University Hospital

    RECRUITING

    Limoges, 87000, France

  • University Medical Center Groningen

    RECRUITING

    Groningen, Netherlands

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