Emergency/Compassionate Use PFO Occluder

Sponsor
Abbott Medical Devices (Industry)
Overall Status
Approved for marketing
CT.gov ID
NCT00584064
Collaborator
(none)

Study Details

Study Description

Brief Summary

Emergency/compassionate use for the AMPLATZER PFO Occluder

Condition or Disease Intervention/Treatment Phase
  • Device: Device closure with the AMPLATZER PFO Occluder

Study Design

Study Type:
Expanded Access

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 60 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Emergency/compassionate use for patients not meeting the inclusion criteria for the AMPLATZER PFO Access Registry.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Abbott Medical Devices

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Abbott Medical Devices
    ClinicalTrials.gov Identifier:
    NCT00584064
    Other Study ID Numbers:
    • AGA-006 - E/C
    First Posted:
    Jan 2, 2008
    Last Update Posted:
    Apr 11, 2019
    Last Verified:
    Apr 1, 2019
    Keywords provided by Abbott Medical Devices
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 11, 2019