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Study identifier: NCT03318406 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-Market BTVA Registry

Condition: Emphysema or COPD  ·  Sponsor: Uptake Medical Technology, Inc.

PhaseN/A
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Bronchoscopic thermal vapor ablation using Uptake Medical Technology Inc.'s InterVapor System is indicated for treatment of patients with heterogeneous upper lobe emphysema. This study is a retrospective and prospective, observational, multi-center, post-market registry of patients prescribed InterVapor. The primary objective of the Registry is to describe the long-term impact of InterVapor treatment on patient quality of life (QOL) in a real-world setting. After InterVapor treatment, patients will be followed for 5 years as per the standard of care and safety and efficacy data (quality of life, pulmonary function, exercise capacity) collected as part of the registry.

This description comes directly from the study's public registry record.

Talk to the study team

Jennifer Idris  ·  +1-408-391-0098  ·  jidris@broncus.com

Always discuss trial participation with your own doctor first.

Locations (20)

Krankenhaus Nord - Klinik FloridsdorfVienna, AustriaRecruiting
Sozialstiftung Bamberg, Klinikum am BruderwaldBamberg, GermanyRecruiting
DRK Kliniken Berlin / MitteBerlin, GermanyRecruiting
FORSCHUNGSINSTITUT Havelhöhe gGmbHBerlin, GermanyRecruiting
Ruhrlandklinik - Westdeutsches Lungenzentrum am Universitätsklinikum Essen gGmbHEssen, GermanyRecruiting
Asklepios Fachkliniken München-GautingGauting, GermanyRecruiting
Martin-Luther-Universität Halle-Wittenberg (Saale)Halle, GermanyRecruiting
Thoraxklinik HeidelbergHeidelberg, GermanyRecruiting
Lungenklinik HemerHemer, GermanyRecruiting
Lungenfachklinik ImmenhausenImmenhausen, GermanyRecruiting
Krankenhaus Martha-Maria MünchenMünchen, GermanyNot Yet Recruiting
Klinikum Nürnberg NordNuremberg, GermanyRecruiting

+ 8 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT03318406