200 Participants Needed

AeriSeal System for Emphysema

(CONVERT_II Trial)

Recruiting at 34 trial locations
AK
CK
JP
Overseen ByJoshua Percy
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to evaluate the AeriSeal System for individuals with severe emphysema and collateral ventilation, which affects air movement in the lungs. The study tests whether sealing specific lung areas can improve breathing when combined with a valve to reduce lung volume. Participants should have severe emphysema with specific lung damage and breathing difficulties. This trial offers an opportunity for those who have stopped smoking and completed pulmonary rehab to explore new treatment options. As an unphased trial, it provides a unique chance for patients to contribute to innovative research and potentially benefit from cutting-edge treatment strategies.

Do I have to stop taking my current medications for the trial?

The trial protocol does not specify if you need to stop taking your current medications. However, you must be on optimal medical management for at least one month before joining the study, and you may need to temporarily stop taking certain blood thinners like heparins and oral anticoagulants before procedures.

What prior data suggests that this method is safe for treating emphysema?

Research has shown that the AeriSeal System is generally safe for people with severe emphysema. In earlier studies, many patients underwent the AeriSeal procedure to block unwanted air paths in the lungs, and the results were encouraging. Most patients improved, with 77.6% experiencing a positive change in their lung condition, making them eligible for further treatment like the Zephyr Valve.

Importantly, the safety data from these studies suggest that the treatment is well-tolerated. No major safety concerns were reported, which is reassuring for anyone considering joining a trial involving AeriSeal. These findings provide confidence in the treatment's safety for those with severe emphysema.12345

Why are researchers excited about this trial?

The AeriSeal system is unique because it aims to treat severe emphysema by blocking collateral ventilation, which is different from the way most current treatments work. Traditional treatments, like bronchodilators and steroids, focus on opening airways and reducing inflammation, but AeriSeal targets the structural problem of air leakage between lung lobes. This innovative approach involves closing lobar fissure gaps, which could improve lung function without the need for more invasive procedures. Researchers are excited because this method could offer a new avenue for patients who haven’t found relief with existing therapies.

What evidence suggests that the AeriSeal procedure is effective for emphysema with collateral ventilation?

Research has shown that the AeriSeal System, which participants in this trial will receive, effectively treats severe emphysema with extra airflow paths in the lungs. Studies found that 77.6% of patients transitioned from having these extra airflow paths to not having them after treatment with AeriSeal Foam. This indicates that the treatment successfully blocked unnecessary airflow in most patients, making them eligible for other procedures like the Zephyr Valve. Clinical data has proven the AeriSeal System safe and effective, with long-term benefits reported. These findings suggest that the AeriSeal System could improve lung function and quality of life for patients with severe emphysema.12567

Who Is on the Research Team?

NS

Narinder Shargill, PhD

Principal Investigator

Pulmonx Corporation

Are You a Good Fit for This Trial?

Inclusion Criteria

You understand what the study involves and agree to take part in it.
You are between 22 and 80 years old when you sign the consent form.
You finished a pulmonary rehabilitation program in the past 6 months.
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

AeriSeal Treatment

Participants undergo the AeriSeal procedure to block collateral ventilation by closing the lobar fissure gaps or collateral air channels.

6 weeks
1 visit (in-person) for the procedure

Follow-up

Participants are monitored for safety and effectiveness after treatment, including conversion of collateral ventilation status and lung volume reduction.

24 months
Regular visits at Day 45, Month 3, Month 6, Month 12, and Month 24

Zephyr Valve Placement

Participants who convert from CV+ to CV- undergo bronchoscopic lung volume reduction with Zephyr Valve.

Ongoing as per standard of care

What Are the Treatments Tested in This Trial?

Interventions

  • AeriSeal System
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: AeriSealExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Pulmonx Corporation

Lead Sponsor

Trials
15
Recruited
1,200+

Citations

News Release - Investor Relations | Pulmonx CorporationCONVERT trial data demonstrate AeriSeal® System is safe and effective with 77.6% of patients converted from CV+ to CV-.
NCT04559464 | Fissure Closure With the AeriSeal System ...The primary AeriSeal endpoint will be the percentage of study subjects that are successfully converted from a positive collateral ventilation status (CV+) in ...
Pulmonx Announces Presentation of Clinical Data from the ...CONVERT trial data demonstrate AeriSeal® System is safe and effective with 77.6% of patients converted from CV+ to CV- 5-year durability ...
CONVERT Trial: Collateral ventilation conversion by closure ...Closure of the fissure gap with AeriSeal Foam (AF) with successful ZV treatment has been reported (Ing A et al. J Bronchol Interven Pulmonl. 2020;27(1):e14).
American Journal of Respiratory and Critical Care MedicineMean data +SD data is presented. Results: 328 patients underwent collateral ventilation assessment; 66 (20%) patients were not eligible due to CV+ status.
NCT06035120 | An Evaluation of the AeriSeal System for ...All enrolled subjects meeting final eligibility will undergo the AeriSeal procedure to block collateral ventilation by closing the lobar fissure gaps or ...
Zephyr Valve benefits previously ineligible patients after ...Conclusions: AeriSeal is safe and effective in occluding collateral channels to convert a CV+ lobe to CV-, allowing emphysema patients with collateral ...
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