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Standard Medical Management in Secondary Prevention of Ischemic Stroke in China (SMART)
This study is currently recruiting participants.
Verified by Peking Union Medical College Hospital, April 2008
Sponsored by: Peking Union Medical College Hospital
Information provided by: Peking Union Medical College Hospital
ClinicalTrials.gov Identifier: NCT00664846
  Purpose

The purposes of the study are to analyse the cross-section data of secondary stroke prevention in China and to carry out a standard medical management including medicine and interactive education program,and to evaluate the efficacy and safety of the standard medical management in secondary stroke prevention.


Condition Intervention
Stroke
Drug: Aspirin / Clopidogrel, Atorvastatin / Simvastatin
Drug: Asprin / Clopidogrel, Atorvastatin / Simvastatin

Drug Information available for: Valsartan Nifedipine Atorvastatin Atorvastatin calcium Glipizide Metformin Metformin hydrochloride Simvastatin Acetylsalicylic acid Amlodipine Amlodipine besylate Clopidogrel Clopidogrel Bisulfate Benazepril Benazepril hydrochloride Indapamide Acarbose
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: Standard Medical Management in Secondary Prevention of Ischemic Stroke in China.

Further study details as provided by Peking Union Medical College Hospital:

Primary Outcome Measures:
  • Success Rate of standard medical management [ Time Frame: 1 year after enrolled ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Ischemic stroke [ Time Frame: 1 year after enrolled ] [ Designated as safety issue: Yes ]
  • Non-fatal acute coronary syndrome [ Time Frame: 1 year after enrolled ] [ Designated as safety issue: Yes ]
  • Transient Ischemic Attack [ Time Frame: 1 year after enrolled ] [ Designated as safety issue: Yes ]
  • Hemorrhagic Stroke [ Time Frame: 1 year after enrolled ] [ Designated as safety issue: Yes ]
  • All-cause Death [ Time Frame: 1 year after enrolled ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 5000
Study Start Date: April 2008
Estimated Study Completion Date: August 2010
Estimated Primary Completion Date: July 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental Drug: Aspirin / Clopidogrel, Atorvastatin / Simvastatin
Standard Medical Management,including antiplatelet agents(Aspirin 75~150mg/day or Clopidogrel 75mg/day),statins(Atorvastatin 20mg/day or Simvastatin 20mg/day),risk factor lowering agents (antihypertension agents:Amlodipine 5mg/day or Benazepril 10mg/day or Valsartan 80mg/day or Nifedipine 30mg/day or Indapamide 2.5mg/day,antidiabetic agents: Metformin 0.5 tid or Glipizide 5mg tid or Acarbose 50mg tid )if necessary,interactive education program (Online medical education program, health behavior guide) .
2: Active Comparator Drug: Asprin / Clopidogrel, Atorvastatin / Simvastatin
Antiplatelet agents(Aspirin 75~150mg/day or Clopidogrel 75mg/day),statins(Atorvastatin 20mg/day or Simvastatin 20mg/day),risk factor lowering agents (antihypertension agents:Amlodipine 5mg/day or Benazepril 10mg/day or Valsartan 80mg/day or Nifedipine 30mg/day or Indapamide 2.5mg/day,antidiabetic agents: Metformin 0.5 tid or Glipizide 5mg tid or Acarbose 50mg tid )if necessary

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Ischemic cerebral infarction or TIA within 30 days.
  2. Aged above 18 years old.
  3. Hospitalized.
  4. Cranial CT or MRI scan exclude intracranial hemorrhagic diseases
  5. Stable clinical and neurological conditions.
  6. A Modified Rankin score less than 4 at enrollment
  7. Informed consent is obtained.

Exclusion Criteria:

Patients will be excluded from entry if any of the criteria listed below are met

  1. Documented stroke caused by conditions other than atherosclerosis, ie, surgical or vascular intervention procedure.
  2. Severe co-morbid or unstable medical condition, ie, heart failure, respiratory failure and renal failure, severe liver dysfunction, malignancy with likelihood of death within the next 2 years
  3. Significant memory or behavioural disorder, ie, Alzheimer disease, etc, daily care needed.
  4. A Modified Rankin score is more than 4
  5. Concurrent participation in another clinical trial
  6. Pregnant
  7. Unable to give informed consent.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00664846

Contacts
Contact: Liying Cui 86-10-6529-6373 pumchcly@yahoo.com.cn
Contact: Bin Peng 86-10-6529-6371 pengbin3@hotmail.com

  Show 48 Study Locations
Sponsors and Collaborators
Peking Union Medical College Hospital
Investigators
Principal Investigator: Liying Cui Peking Union Medical College Hospital
  More Information

Responsible Party: Peking Union Medical College Hospital ( Liying Cui )
Study ID Numbers: 2006BAI01A10-1
Study First Received: April 12, 2008
Last Updated: May 20, 2008
ClinicalTrials.gov Identifier: NCT00664846  
Health Authority: China: Ministry of Health

Keywords provided by Peking Union Medical College Hospital:
Stroke
Prevention Therapy

Study placed in the following topic categories:
Indapamide
Glipizide
Cerebral Infarction
Simvastatin
Metformin
Stroke
Vascular Diseases
Central Nervous System Diseases
Ischemia
Brain Diseases
Nifedipine
Cerebrovascular Disorders
Amlodipine
Acarbose
Aspirin
Clopidogrel
Benazepril
Neoplasm Metastasis
Brain Ischemia
Brain Infarction
Infarction
Valsartan
Atorvastatin

Additional relevant MeSH terms:
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Antilipemic Agents
Therapeutic Uses
Hematologic Agents
Nervous System Diseases
Enzyme Inhibitors
Platelet Aggregation Inhibitors
Cardiovascular Diseases
Anticholesteremic Agents
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009