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Post Market Observational, Prospective, Multi-center Study

NCT01806636 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 1275

Last updated 2021-07-16

No results posted yet for this study

Summary

This registry is a post market observational, prospective, multi-center registry.

It is designed to evaluate patient experience with the endobronchial coil system for the relief of the emphysema symptoms and the continued collection of safety and effectiveness data on this CE Mark product.

Conditions

  • Emphysema

Interventions

DEVICE

PneumRx Coil System

Sponsors & Collaborators

  • PneumRx, Inc.

    collaborator INDUSTRY

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Martin Hetzel, Prof. · Krankenhaus vom Roten Kreuz

  • Christian Schumann, MD · Klinikenverbund Kempten-Oberallgäu

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2019-07-31
Completion
2019-07-31

Countries

  • Austria
  • Denmark
  • Germany
  • Spain
  • Switzerland
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01806636 on ClinicalTrials.gov