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NCT01397175: CHOICE

BES, EES, and ZES-R in Real World Practice

Terminated NA Last updated 9 July 2019
What this trial tests

NA trial testing Biolimus-eluting stent in Coronary Artery Disease in 1,960 participants. Terminated before completion.

Timeline
16 January 2013
Primary endpoint
5 December 2017
1 January 2019

Quick facts

Lead sponsorYonsei University
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment1,960
Start date16 January 2013
Primary completion5 December 2017
Estimated completion1 January 2019
Sites5 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Yonsei University

Who can join

18 and older, any sex, with Coronary Artery Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this study is to compare the rate of device-oriented composite consisted of cardiac death, myocardial infarction not clearly attributable to a nontarget vessel, and clinically indicated target lesion revascularization among the patients treated with EES, ZES-R, or BES at 24-month clinical follow-up post-index procedure. Trial end points are summarized in Table I. The hypothesis is that BES is equivalent to EES or BES is equivalent to ZES-R at the primary end point.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Randomized Comparison of Everolimus- and Zotarolimus-Eluting Coronary Stents With Biolimus-Eluting Stents in All-Comer Patients.
    Youn YJ, Lee JW, Ahn SG, Lee SH, et al · · 2020 · cited 5× · PMID 32160779 · DOI 10.1161/circinterventions.119.008525

Verify or expand the search:

Other recruiting trials for Coronary Artery Disease

Currently open trials in the same condition.

Other Yonsei University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01397175.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing