About this trial

The goal of this clinical trial is to learn if bronchoscopic lung volume reduction with endobronchial thermal liquid ablation (ETLA) works to treat severe emphysema in terms of feasibility and safety.

Participants will:

* Have up to two ETLA procedures * Complete five clinic follow-up visits and two virtual follow-up visits.

Eligibility criteria

Qualifiers

Age ≥ 40 years old

Diagnosis of COPD with FEV1/FVC less than 0.7 post-bronchodilation

Post-bronchodilator Forced Expiratory Volume (FEV1) ≥ 20% and ≤ 49% of predicted value

Total lung capacity (TLC) ≥ 100% predicted

Disqualifiers

Body mass index (BMI) < 16 kg/m² or ≥ 33 kg/m²

DLCO < 20% predicted

Chronic bronchitis as defined by cough and sputum production for at least 3 months per year for two consecutive years, in the absence of other conditions that can explain these symptoms

75ml or greater sputum production per day most days of the week

Trial design

Treatments tested in this trial

  • Endobronchial Therman Liquid Ablation (ETLA)

Treatment groups

30 Participants
are divided into 1 treatment group

Locations

7
Austria
Klinik Floridsdorf1210, ViennaAustria, Austria
Universitätsklinikum Allgemeines Krankenhaus Wien1090, ViennaAustria, Austria
Germany
Gemeinschaftskrankenhaus Havelhöhe gGmbH Klinik für Anthroposophische Medizin14089, BerlinGermany, Germany
Asklepios Lungenklinik Gauting GmbH82131, GautingGermany, Germany

Sponsors and collaborators

Morair Medtech, LLC

Lead sponsor