Last updated on July 2018

Post Market Observational Prospective Multi-center Study

Brief description of study

This registry is a post market observational, prospective, multi-center registry. It is designed to evaluate patient experience with the RePneu device for the relief of the emphysema symptoms and the continued collection of safety and effectiveness data on this CE Mark product. In addition, the registry will collect information that will serve as the foundation for a cost effectiveness analysis.

Clinical Study Identifier: NCT01806636

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Jozef Tanczos

Donaueschingen, Germany
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