LVRC IDE RePneu Crossover Study

Investigator: Timothy Connolly, MD

Study Coordinator: Liliana Calderon

Status: Open Not Enrolling Number: NCT01806636

Phone: 713.441.3958

Protocol Number: Pro00012717


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.
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