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NCT04186546

Zephyr Valve Registry (ZEVR)

Sponsor: Pulmonx Corporation

View on ClinicalTrials.gov

Summary

The purpose of this Post-Approval Registry is to gather ongoing safety and effectiveness assessment of the Zephyr Valve treatment in a real-world setting.

Official title: Zephyr Valve Registry

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

150

Start Date

2019-11-25

Completion Date

2026-12-31

Last Updated

2025-04-29

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Zephyr Valve Procedure

The Pulmonx Zephyr Endobronchial Valve is an implantable bronchial valve intended to decrease volume in targeted regions of the lung. It is indicated for the treatment of patients with severe emphysema. The Zephyr Valves are placed in the diseased region of the lung using bronchoscopy. As the diseased region of the lung shrinks in size, healthier regions may expand and function more efficiently, resulting in improved breathing.

Locations (11)

University of Alabama at Birmingham

Birmingham, Alabama, United States

University of Chicago

Chicago, Illinois, United States

Northwestern Medicine

Winfield, Illinois, United States

Henry Ford Hospital

Detroit, Michigan, United States

The Lung Center

DuBois, Pennsylvania, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

Temple University Hospital

Philadelphia, Pennsylvania, United States

University of Pittsburgh School of Medicine

Pittsburgh, Pennsylvania, United States

Houston Methodist

Houston, Texas, United States

Inova Health

Fairfax, Virginia, United States

Froedtert Memorial-Medical College of Wisconsin

Milwaukee, Wisconsin, United States