AIFSIDDES: Angiographic and Intravascular Ultrasound (IVUS) Follow-up After Simultaneously Implanted Different Drug-eluting Stents in Same Individuals

Sponsor
Liuhuaqiao Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT00973375
Collaborator
(none)
30
1

Study Details

Study Description

Brief Summary

The purpose of this study is to investigate if there is any different follow-up results by angiography and IVUS between two different drug-eluting stents after implanted simultaneously in same individuals.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    30 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Study Start Date :
    May 1, 2009

    Arms and Interventions

    Arm Intervention/Treatment
    Endeavor group and Excel group

    Endeavor group: measurements from the vessels implanted Endeavor stent(s). Excel group: measurements from the vessels implanted Excel stent(s).

    Outcome Measures

    Primary Outcome Measures

    1. Segment and instent restenosis measured by coronary angiography and IVUS. [at 12 months after implantation]

    Secondary Outcome Measures

    1. Uncovered and malposition of stent. [at 12 months after implantation.]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • These patients who received two kinds of drug-eluting stent (Endeavor and Excel) im simultaneously.
    Exclusion Criteria:
    • Dual anti-platelet therapy less than 12 months.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Liuhuaqiao Hospital Guangzhou Guangdong China 510010

    Sponsors and Collaborators

    • Liuhuaqiao Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00973375
    Other Study ID Numbers:
    • LHQ09-003
    First Posted:
    Sep 9, 2009
    Last Update Posted:
    Sep 9, 2009
    Last Verified:
    Sep 1, 2009

    Study Results

    No Results Posted as of Sep 9, 2009