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UnknownNCT02014818

Multicenter Comparison of Early and Late Vascular Responses to Everolimus-eluting Cobalt-CHromium Stent

Multicenter Comparison of Early and Late Vascular Responses to Everolimus-eluting Cobalt-CHromium Stent and Platelet AggregatioN Studies In Patients With Stable Angina Managed as Elective Case : MECHANISM-Elective

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
104 (actual)
Sponsor
Kobe University · Industry
Sex
All
Age
20 Years – 84 Years
Healthy volunteers
Not accepted

Summary

To treat patients with stable coronary artery disease, elective percutaneous coronary intervention (PCI) will be performed with the use of an everolimus-eluting cobalt- chromium stent (everolimus-eluting stent: EES, Xience Prime, Xpedition), which is the current standard drug-eluting stent (DES). Vascular responses at the site of stent placement will be evaluated by optical coherence tomography (OCT) at 1 or 3 months and at 12 months after stent placement, along with observation of changes over time in the target vessel. The relationships between OCT findings and the time course of platelet aggregation and between OCT findings and the occurrence of major cardio- cerebrovascular events will also be elucidated.

Conditions

Interventions

TypeNameDescription
DEVICECoCr-EES

Timeline

Start date
2014-01-01
Primary completion
2017-12-31
Completion
2018-12-31
First posted
2013-12-18
Last updated
2017-10-18

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT02014818. Inclusion in this directory is not an endorsement.

Multicenter Comparison of Early and Late Vascular Responses to Everolimus-eluting Cobalt-CHromium Stent (NCT02014818) · Clinical Trials Directory