Post Market Observational, Prospective, Multi-center Study

Boston Scientific

Status: Terminated

Conditions: Emphysema

Treatments: Device: PneumRx Coil System

Study type: Observational

Funder types: Industry

Identifiers

NCT01806636

CLN0014

Details and patient eligibility

About

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.

Enrollment: 1,275 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion and exclusion criteria in the Registry are based on CE Mark approved indication and approved Instructions for Use. Patients enrolled and treated in the Registry study should meet the requirements of the PneumRx Endobronchial Coil System Instructions for Use.

Trial design

1,275 participants in 1 patient group

Treatment

Description:

Patients treated with PneumRx Coil System

Treatment:

Device: PneumRx Coil System