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Xience/Promus for Long Coronary Lesion Registry

A Multi Center Registry to Evaluate Multiple Stenting Using by Everolimus-eluting Stents for Treatment of Long Coronary Artery Disease

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01147237
Acronym
XILLION
Enrollment
450
Registered
2010-06-22
Start date
2010-02-28
Completion date
2012-12-31
Last updated
2010-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Long Coronary Artery Disease

Brief summary

The utilization of everolimus-eluting coronary stents in a coronary artery diseases is effective in reducing both repeat revascularization and major adverse cardiac events within two year follow-up. To evaluate the procedural, short and long term clinical outcomes of multiple everolimus-eluting coronary stent implantation in long (\>30mm) coronary lesions.

Interventions

Everolimus-eluting stent implantation in patients with long coronary artery disease

Sponsors

Society for Advancement of Coronary Intervention Research
Lead SponsorNETWORK

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Age ≥20 years and are able to undergo CABG 2. Females who are not pregnant 3. Patients who present with angina symptoms or myocardial ischemia 4. Patients available for post-procedural observation and coronary angiography at 24 months 5. Patients who have signed patient informed consent 6. Lesion length is more than 30mm 7. De novo lesion or non-stented restenosed lesion

Exclusion criteria

1. Patients contraindicated for antiplatelet therapy or anticoagulant therapy 2. Patients with significant allergic reaction to contrast medium 3. Chronic total occlusion 4. Lesion with TIMI0 5. Patients with chronic renal failure (SCr\>3.0mg/dl) -

Design outcomes

Primary

MeasureTime frame
Target lesion revascularization rate1 year

Secondary

MeasureTime frameDescription
Angiographic restenosis9 months
Target vessel revascularization1 year
Technical successInitial
Incidences of acute, sub acute, and late stent thrombosis2 year
Incidence of MACCE2 yeardefined as cardiac death, nonfatal acute myocardial infarction and cerebrovascular events
Target lesion revascularization2 year

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026