A Registry Study of the AeriSeal® System or Lung Volume Reduction in Patients With Advanced Emphysema
NCT01449175 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 54
Last updated 2013-11-14
Summary
The purpose of this study is to provide post market clinical follow-up (PMCF) to obtain long term safety and efficacy information about the AeriSeal System treatment in patients with advanced emphysema.
Conditions
- Chronic Pulmonary Obstructive Disease
- Emphysema
Sponsors & Collaborators
-
Aeris Therapeutics
lead INDUSTRY
Eligibility
- Min Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-01-31
- Primary Completion
- 2013-11-30
- Completion
- 2013-11-30
Countries
- Austria
- France
- Germany
- Israel
Study Locations
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