Last updated on August 2019

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

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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