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Related Studies
Efficacy and Safety of Adding Clopidogrel to Aspirin or Use of Metoprolol in Myocardial Infarction
This study has been completed.
First Received: September 13, 2005   Last Updated: May 4, 2006   History of Changes
Sponsors and Collaborators: University of Oxford
Sanofi-Aventis
AstraZeneca
Information provided by: University of Oxford
ClinicalTrials.gov Identifier: NCT00222573
  Purpose

COMMIT/CCS2 is a large randomised trial of the effects of clopidogrel plus Aspirin versus Aspirin alone in acute heart disease. Patients presenting within 24 hours of the onset of suspected acute MI were potentially eligible provided they were thought to have ST elevation or other ischaemic ECG abnormality with no clear indication for, or contraindication to, trial treatment. All patients were to be given 162 mg ASA daily and, in addition, 75 mg clopidogrel daily or matching placebo for 4 weeks or until prior discharge or death. (Patients were also randomised separately in a 2 X 2 factorial design between metoprolol versus placebo.) The two main study endpoints are death and the composite outcome of death, non-fatal reinfarction or stroke during the scheduled treatment period in hospital.


Condition Intervention Phase
Acute Myocardial Infarction
Drug: clopidogrel and metoprolol
Phase IV

MedlinePlus related topics: Heart Attack
Drug Information available for: Metoprolol Metoprolol Tartrate Metoprolol succinate Clopidogrel Metoprolol fumarate Clopidogrel Bisulfate
U.S. FDA Resources
Study Type: Interventional
Study Design: Double-Blind, Factorial Assignment, Placebo Control, Randomized, Safety/Efficacy Study, Treatment
Official Title: Clopidogrel Or Metoprolol in Myocardial Infarction Trial

Further study details as provided by University of Oxford:

Primary Outcome Measures:
  • Death and the composite outcome of death, non-fatal reinfarction or stroke

Secondary Outcome Measures:
  • Major cardiovascular events

Estimated Enrollment: 46000
Study Start Date: July 1999
Estimated Study Completion Date: February 2005
  Show Detailed Description

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients presenting with ST elevation, left bundle branch block or ST depression within 24 hours of the onset of the symptoms of suspected acute MI

Exclusion Criteria:

  • clear indications for, or contraindications to, any of the study treatments
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00222573

Locations
China
Institute of Cadiovascular diseases, Fuwai hospital, Chinese academy of medical sciences
Beijing, China, 100037
United Kingdom
Clinical Trial Service Unit and Epidemiological Studies Unit
Oxford, United Kingdom, OX3 7LF
Sponsors and Collaborators
University of Oxford
Sanofi-Aventis
AstraZeneca
Investigators
Study Chair: Rory Collins, Msc University of Oxford
Study Chair: Lisheng Liu, MD Institute of cardiovascular diseases, Fuwai hospital, Chinese academy of medical sciences
  More Information

Additional Information:
Publications of Results:
Publications automatically indexed to this study:
Study ID Numbers: COMMIT-CCS2, H6RDCN0
Study First Received: September 13, 2005
Last Updated: May 4, 2006
ClinicalTrials.gov Identifier: NCT00222573     History of Changes
Health Authority: China: Ministry of Health

Keywords provided by University of Oxford:
clopidogrel
metoprolol
myocardial infarction
randomised trial

Study placed in the following topic categories:
Neurotransmitter Agents
Heart Diseases
Adrenergic Agents
Myocardial Ischemia
Vascular Diseases
Cardiovascular Agents
Ischemia
Antihypertensive Agents
Metoprolol
Necrosis
Aspirin
Clopidogrel
Metoprolol succinate
Adrenergic beta-Antagonists
Platelet Aggregation Inhibitors
Adrenergic Antagonists
Anti-Arrhythmia Agents
Infarction
Myocardial Infarction

Additional relevant MeSH terms:
Neurotransmitter Agents
Adrenergic Agents
Molecular Mechanisms of Pharmacological Action
Myocardial Ischemia
Hematologic Agents
Physiological Effects of Drugs
Necrosis
Pathologic Processes
Therapeutic Uses
Adrenergic beta-Antagonists
Cardiovascular Diseases
Anti-Arrhythmia Agents
Myocardial Infarction
Sympatholytics
Heart Diseases
Vascular Diseases
Ischemia
Cardiovascular Agents
Metoprolol
Antihypertensive Agents
Pharmacologic Actions
Autonomic Agents
Clopidogrel
Metoprolol succinate
Platelet Aggregation Inhibitors
Adrenergic Antagonists
Peripheral Nervous System Agents
Infarction

ClinicalTrials.gov processed this record on March 16, 2009