Now Enrolling

Do you have COPD and struggle with severe emphysema?

You may be eligible to participate in a clinical research study evaluating a small, spring like implant designed to help people with severe emphysema breathe easier.

Check eligibility
Investigational use only
Voluntary participation
Compensation provided
About the study

What is the BREATHE-3 clinical trial?

BREATHE-3 is a research study designed to assess the safety and efficacy of the Apreo BREATHE Airway Scaffold — a small implant placed in the lung and designed to gently tent open blocked airways, helping trapped air escape which may make it easier to breathe.

The implant in action

See how the BREATHE Airway Scaffold opens the airway

The Apreo BREATHE Airway Scaffold is designed to gently tent open blocked airways, helping trapped air escape which may make it easier to breathe.

CAUTION — Investigational Device. Limited by United States law to investigational use. Exclusively for clinical investigation.

Participation criteria

Who may be eligible?

Study participants must meet the below criteria.

Diagnosed with COPD or severe emphysema by a doctor

Currently receiving optimal medical management

Not actively smoked within 4 months and agrees to smoking cessation

Not significantly immunocompromised

Reduced lung function, even when using an inhaler or bronchodilator

Between 40 and 84 years of age

Willing and able to complete a supervised pulmonary rehab program or have already completed in the prior year

No prior lung surgery or implant in place

View the complete inclusion & exclusion criteria for study NCT06891755 on ClinicalTrials.gov.

View on ClinicalTrials.gov
How it works

What to expect from pre-screen to treatment

1
Check your eligibility

Answer a series of pre-screening questions to see if you may be a fit for the study. Start here →

About 10 minutes
2
Connect with a study coordinator

A study coordinator near you will follow up to explain the study and schedule appointments to assess your eligibility.

3
Receive randomized treatment

Participants will be randomized to the BREATHE Airway Scaffold plus optimal medical therapy or optimal medical therapy alone. The control group may cross over after the 12-month follow-up visit.

2 of 3

participants are randomized to receive the implant

12-month observation periodVisits at months 1, 3, 6 & 12
4
Follow-up

Participants are monitored for safety and efficacy after treatment.

3 yearsVisits at years 2 & 3
5
Crossover option (control group)

Control group participants may choose to receive the BREATHE treatment after their 12-month follow-up visit.

12 - 15 months from baseline Follow-ups at 7 days, 1 month & 6 months post procedure
Check eligibility
Quick pre-screen survey

Check eligibility

Thank you for your interest in this clinical study. The questions below will help determine whether the study might be an option for you.