Feasibility Study of PneumRx's Lung Volume Reduction Coil (LVRC)

NCT01328899 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2021-07-21

No results posted yet for this study

Summary

This is a multicenter single arm open label study. The primary objective is to evaluate the safety and effectiveness of the Lung Volume Reduction Coil (LVRC) for the treatment of patients with emphysema in multiple centers.

Conditions

  • Emphysema

Interventions

DEVICE

Lung Volume Reduction Coil (LVRC) (PneumRx's)

Lung Volume Reduction Coil

Sponsors & Collaborators

  • PneumRx, Inc.

    collaborator INDUSTRY
  • Boston Scientific Corporation

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • France
  • Germany
  • Netherlands

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 NCT01328899 on ClinicalTrials.gov