NCT00973375

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2009

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

September 8, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 9, 2009

Completed
Last Updated

September 9, 2009

Status Verified

September 1, 2009

First QC Date

September 8, 2009

Last Update Submit

September 8, 2009

Conditions

Keywords

Drug-eluting stentcoronary restenosiscoronary thrombosis

Outcome Measures

Primary Outcomes (1)

  • Segment and instent restenosis measured by coronary angiography and IVUS.

    at 12 months after implantation

Secondary Outcomes (1)

  • Uncovered and malposition of stent.

    at 12 months after implantation.

Study Arms (1)

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).

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

These patients who received two kinds of drug-eluting stent (Endeavor and Excel) im simultaneously.

You may qualify if:

  • These patients who received two kinds of drug-eluting stent (Endeavor and Excel) im simultaneously.

You may not qualify if:

  • Dual anti-platelet therapy less than 12 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Liuhuaqiao Hospital

Guangzhou, Guangdong, 510010, China

RECRUITING

Related Publications (3)

  • Waseda K, Miyazawa A, Ako J, Hasegawa T, Tsujino I, Sakurai R, Yock PG, Honda Y, Kandzari DE, Leon MB, Fitzgerald PJ; ENDEAVOR IV Trial Investigators. Intravascular ultrasound results from the ENDEAVOR IV trial: randomized comparison between zotarolimus- and paclitaxel-eluting stents in patients with coronary artery disease. JACC Cardiovasc Interv. 2009 Aug;2(8):779-84. doi: 10.1016/j.jcin.2009.05.015.

    PMID: 19695548BACKGROUND
  • Lee CH, Zhang J, Kailasam A, Tai BC, Ye F, Low AF, Hou X, Hay ET, Teo SG, Lim YT, Chen S, Tan HC. An intravascular ultrasound study of Cypher, Taxus, and endeavor stents on relation between neointimal proliferation and residual plaque burden. J Interv Cardiol. 2008 Dec;21(6):519-27. doi: 10.1111/j.1540-8183.2008.00397.x. Epub 2008 Oct 21.

    PMID: 18973509BACKGROUND
  • Miyazawa A, Ako J, Hongo Y, Hur SH, Tsujino I, Courtney BK, Hassan AH, Kandzari DE, Honda Y, Fitzgerald PJ; ENDEAVOR III Investigators. Comparison of vascular response to zotarolimus-eluting stent versus sirolimus-eluting stent: intravascular ultrasound results from ENDEAVOR III. Am Heart J. 2008 Jan;155(1):108-13. doi: 10.1016/j.ahj.2007.08.008. Epub 2007 Sep 14.

    PMID: 18082499BACKGROUND

MeSH Terms

Conditions

Coronary RestenosisCoronary Thrombosis

Condition Hierarchy (Ancestors)

Coronary StenosisCoronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesThrombosisEmbolism and Thrombosis

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 8, 2009

First Posted

September 9, 2009

Study Start

May 1, 2009

Last Updated

September 9, 2009

Record last verified: 2009-09

Locations