Evaluation of the First, Second, and New Drug-Eluting Stents in Routine Clinical Practice

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age19+
SponsorSeung-Jung Park

About this trial

The objective of this study is to evaluate effectiveness and safety of the new drug-eluting stent (DES), as compared with the first-,second-,third-, and fourth-generation DES, in the "real world" daily practice.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

coronary disease amenable to percutaneous coronary intervention (PCI)

no clinical and lesion limitations

Disqualifiers

patients with a mixture of several DES

terminal illness with life expectancy less than 1 year

patients with cardiogenic shock

Trial population

consecutive patients amenable to PCI

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

50,000 Participants
are grouped into 27 trial groups

27

Trial groups

See each trial group below.

Group A: DESSIAN
Group B: K-XIENCE
Group C: GENOUS
Group D: ELEMENT
Group E: PRIME
Group F: NOBORI
Group G: INTEGRITY
Group H: XPEDITION
Group I: BIOMATRIX
Group J: CILOTAX
Group K: DEB
Group L: DESYNE
Group M: PREMIER
Group N: ORSIRO
Group O: ONYX
Group P: BVS
Group Q: BVS AMI
Group R: Ultimaster
Group S: Synergy
Group T: Biofreedom
Group U: Firehawk
Group V: DESyne X2
Group W: Sierra
Group X: Tansei
Group Y: Synergy XD and Synergy Megatron™
Group Z: Xience-Skypoint
Group [: Coroflex ISAR NEO

Trial outcomes

Primary outcomes

1

Composite of death, nonfatal myocardial infarction (MI), or ischemic-driven Target- Vessel Revascularization (TVR)

Time frame
at 12 months post procedure

Secondary outcomes

1

Death (all-cause and cardiac)

Time frame
at 12 months and annually up to 5 years
2

Myocardial infarction

Time frame
at 12 months and annually up to 5 years
3

Stent thrombosis

Time frame
at 12 months and annually up to 5 years
4

Target-lesion and target-vessel revascularization

Time frame
at 12 months and annually up to 5 years

Other outcomes

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Korean centresRecruiting Multiple LocationsSouth Korea

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Seung-Jung Park

Lead sponsor

CardioVascular Research Foundation, Korea

Sponsor institution

CardioVascular Research Foundation, Korea

Collaborator