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Spiration IBV® Valve System and Spiration Airway Sizing Kit

NCT01872312 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2022-06-30

No results posted yet for this study

Summary

This procedure allows patients to use the Humanitarian Use Device, IBV® Valve System.

Conditions

  • Management of BPF (Bronchopleural Fistulae)

Interventions

DEVICE

treatment with valves (The Spiration® IBV Valve System)

treat BPF

Sponsors & Collaborators

  • Olympus Corporation of the Americas

    collaborator INDUSTRY

  • Ohio State University

    lead OTHER

Principal Investigators

  • shaheen Islam, MD · Ohio State University

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-25
Primary Completion
2014-02-14
Completion
2014-02-14

Countries

  • United States

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 NCT01872312 on ClinicalTrials.gov