LVRC IDE RePneu Crossover Study

Investigator: Timothy Connolly, MD

Study Coordinator: Alice Pavlak

Status: Open Not Enrolling

ClinicalTrials.gov Number: NCT01806636

Phone: 713..44.1.3246

IRB Number: Pro00012717

Description

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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