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The Application of Ticagrelor Combined With Low Molecular Weight Heparin During PCI

The Application of Ticagrelor Combined With Low Molecular Weight Heparin During PCI

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02658838
Enrollment
300
Registered
2016-01-20
Start date
2015-04-30
Completion date
2017-09-30
Last updated
2016-01-20

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

Conditions

LOVASTATIN/TICAGRELOR [VA Drug Interaction]

Brief summary

The purpose of this study is to determine ticagrelor combining with low molecular weight heparin is effective and safe during PCI or not.

Detailed description

Ticagrelor is a new drug compared with clopidogrel. It has a stronger antiplatelet capacity. After PCI,whether using low molecular weight heparin can make patients better prognosis or not, What's more,full amount or half amount low molecular weight heparin?, also investigators want to explore that whether it may lead to more bleeding events.

Interventions

DRUGTicagrelor

Patients were treated with full amount low molecular weight heparin randomly after PCI,All patients are treated with ticagrelor one year.

DRUGfull amount low molecular weight heparin

Patients were treated with half amount low molecular weight heparin randomly after PCI,All patients are treated with ticagrelor one year.

DRUGhalf amount low molecular weight heparin

Patients were treated with half amount low molecular weight heparin randomly after PCI,All patients are treated with ticagrelor one year.

DRUGNo low molecular weight heparin

Patients were treated with no low molecular weight heparin randomly after PCI,All patients are treated with ticagrelor one year.

Sponsors

Beijing Anzhen Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age ≥18 years old and ≤75 years ; 2. unstable angina, non-ST segment elevation acute myocardial infarction, old myocardial infarction, or confirm the presence of myocardial ischemia; 3. voluntary participation in clinical trials, and informed consent;

Exclusion criteria

1. acute ST segment elevation myocardial infarction, stable angina pectoris; 2. aspirin allergy or resistance; 3. consolidated stroke, chronic obstructive pulmonary disease and other ticagrelor contraindications; 4. patients have coagulopathy; 5. can not be continued for one year with aspirin and treatment of dual antiplatelet ticagrelor; 6. can not complete revascularization; 7. NYHA ≥Ⅲ level or left ventricular ejection fraction \<40%; 8. severe liver and kidney dysfunction (ALT and AST were more than three times the upper limit of normal, creatinine clearance less than 30ml / min-1.1.72m-2);

Design outcomes

Primary

MeasureTime frame
all cause mortalityone year

Secondary

MeasureTime frameDescription
Nonfatal myocardial infarctionone yearPatients occur acute myocardial infarction in a year,but it could not lead to die.
Non-fatal strokeone yearPatients occur stroke in a year,but it could not lead to die.
Revascularization againone yearCoronary arteries occur stenosis again in a year,the patients are treated with revascularization,including PCI and CABG.
Rehospitalization for ACS or heart failureone yearPatients are hospitalized again because of ACS or heart failure in a year.
Bleeding eventsone yearassessing the bleeding events according the TIMI grade.

Countries

China

Outcome results

None listed

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