This registry is a post market observational, prospective, multi-center registry. It is designed to evaluate patient experience with the endobronchial coil system for the relief of the emphysema symptoms and the continued collection of safety and effectiveness data on this CE Mark product.
Study Type
OBSERVATIONAL
Enrollment
1,275
Changes in Quality of Life (QOL) measures
Time frame: 6 months and yearly up to three years post treatment 1
Changes in Pulmonary Function and Exercise Capacity test results
Time frame: 6 months and yearly up to three years post treatment 1
Safety including any device malfunction or failure(s)
Time frame: 6 months and yearly up to three years post treatment 1
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Otto-Wagner-Spital
Vienna, Austria
Rigshospitalet Copenhaven
Copenhagen, Denmark
Hochtaunus-Kliniken, Klinik für Pneumolog und Onkologie
Bad Homburg, Germany
Charité Campus Mitte
Berlin, Germany
Charité Campus Virchow-Klinikum
Berlin, Germany
Gemeinschaftskrankenhaus Havelhöhe
Berlin, Germany
Helios Klinikum Emil von Behring, Berlin
Berlin-Zehlendorf, Germany
Universitätsklinikum Bonn
Bonn, Germany
Ev. Krankenhaus Göttingen-Weende
Bovenden, Germany
DRK Klinik am Bürgerpark
Bremerhaven, Germany
...and 63 more locations