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Effects of Atorvastatin Versus Pravastatin on Platelet Inhibition by Clopidogrel
This study has been completed.
First Received: November 28, 2006   Last Updated: November 6, 2008   History of Changes
Sponsor: Shenyang Northern Hospital
Information provided by: Shenyang Northern Hospital
ClinicalTrials.gov Identifier: NCT00405717
  Purpose

Clopidogrel and statins are frequently coadministered in patients with ischemic heart diseases. Recent reports suggested that clopidogrel's effectiveness in inhibiting adenosine diphosphate (ADP)-induced platelets aggregation is attenuated by co-administration of certain statins. The objective of the present study is to define which kind of statins might interfere with the antiaggregation property of clopidogrel in patients with acute coronary Syndrome after percutaneous coronary intervention (PCI).

In this prospective randomized study, all patients in test group will receive clopidogrel plus atorvastatin, and all patients in control group will receive clopidogrel plus pravastatin. All patients will be followed up for one year. The primary endpoints include death, non fatal AMI, urgent revascularization. The secondary endpoints include hemorrhage events and subacute thrombosis events at 1 year.


Condition Intervention Phase
Ischemic Heart Disease
Acute Coronary Syndromes
Drug: atorvastatin,pravastatin
Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: Effects of Atorvastatin Versus Pravastatin on Platelet Inhibition by Clopidogrel in Patients With Acute Coronary Syndrome After Percutaneous Coronary Intervention

Resource links provided by NLM:


Further study details as provided by Shenyang Northern Hospital:

Primary Outcome Measures:
  • major adverse cardiac and cerebral events at 1 year [ Time Frame: 1 year ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • hemorrhage events and subacute thrombosis events at 1 year [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 1300
Study Start Date: February 2006
Study Completion Date: May 2008
Primary Completion Date: May 2008 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosed with ACS.
  • Between ages of 18 Years and 85 years.
  • Presence of one or several stenosis in native coronary arteries requiring PCI.
  • Willing and able to sign informed consent.

Exclusion Criteria:

  • A history of bleeding diathesis.
  • New York Heart Association functional class IV.
  • Prior PCI or coronary bypass grafting < 3 months.
  • Contraindications to statins, clopidogrel and aspirin (White blood cells counts < 4×109/L or platelet counts <100 g/l; creatinine clearance <25 ml/ min; active liver disease).
  • Use of glycoprotein IIb/IIIa inhibitors before PCI.
  • Use of statins before PCI.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00405717

Locations
China, Liaoning
Northern Hospital
shenyang, Liaoning, China
Sponsors and Collaborators
Shenyang Northern Hospital
Investigators
Principal Investigator: Yaling Han, M.D. Shenyang Northern Hospital
  More Information

No publications provided

Responsible Party: Shenyang Northern Hospital ( Yaling Han )
Study ID Numbers: NH-2006-C002
Study First Received: November 28, 2006
Last Updated: November 6, 2008
ClinicalTrials.gov Identifier: NCT00405717     History of Changes
Health Authority: China: Ministry of Health

Keywords provided by Shenyang Northern Hospital:
ischemic heart disease
acute coronary syndromes
percutaneous transluminal coronary angioplasty
statin
clopidogrel

Additional relevant MeSH terms:
Antimetabolites
Heart Diseases
Disease
Molecular Mechanisms of Pharmacological Action
Antilipemic Agents
Myocardial Ischemia
Hematologic Agents
Vascular Diseases
Enzyme Inhibitors
Anticholesteremic Agents
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Pharmacologic Actions
Pravastatin
Pathologic Processes
Therapeutic Uses
Syndrome
Clopidogrel
Acute Coronary Syndrome
Cardiovascular Diseases
Platelet Aggregation Inhibitors
Atorvastatin

ClinicalTrials.gov processed this record on February 08, 2010