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JASAP: Japanese Aggrenox Stroke Prevention vs. Aspirin Programme
This study is ongoing, but not recruiting participants.
Study NCT00311402   Information provided by Boehringer Ingelheim Pharmaceuticals
First Received: March 28, 2006   Last Updated: April 22, 2009   History of Changes
This Tabular View shows the required WHO registration data elements as marked by

March 28, 2006
April 22, 2009
April 2006
Recurrence of brain infarction (fatal or non-fatal) [ Time Frame: 52 weeks to 124 weeks ]
Recurrence of brain infarction (fatal or non-fatal) [ Time Frame: 52 weeks to 124 weeks ]
Complete list of historical versions of study NCT00311402 on ClinicalTrials.gov Archive Site
Brain hemorrhage Subarachnoid hemorrhage Transient ischemic attack (TIA) Acute coronary syndromes (myocardial infarction, angina unstable, cardiac death) Other vascular events [ Time Frame: 52 weeks to 124 weeks ]
Brain hemorrhage Subarachnoid hemorrhage Transient ischemic attack (TIA) Acute coronary syndromes (myocardial infarction, angina unstable, cardiac death) Other vascular events [ Time Frame: 52 weeks to 124 weeks ]
 
JASAP: Japanese Aggrenox Stroke Prevention vs. Aspirin Programme
JASAP: Japanese Aggrenox Stroke Prevention vs. Aspirin Programme, Phase III Study to Compare the Preventive Effect of Recurrent Brain Infarction and Safety of Aggrenox (Combination Drug Containing Sustained-Release Dipyridamole 200 mg/Acetylsalicylic Acid 25 mg) Twice Daily vs. Acetylsalicylic Acid 81 mg Once Daily

Phase III study to compare the preventive effect of recurrent brain infarction and safety of Aggrenox (combination drug containing sustained-release dipyridamole 200 mg/acetylsalicylic acid 25 mg) twice daily vs. acetylsalicylic acid 81 mg once daily

 
Phase III
Interventional
Prevention, Parallel Assignment
Cerebrovascular Accident
  • Drug: Aggrenox capsule
  • Drug: ASA 81 mg tablet
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
1250
 
February 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

Patients with a diagnosis of cerebral infarction (excluding cardiogenic cerebral embolism) who meet the diagnostic criteria based on the National Institute of Neurological Disorders and Stroke (NINDS) ad hoc committee¿s classification of cerebrovascular disease III.

  1. Patients who have had an onset of cerebral infarction, the time of which is known, between 1 week and 6 months before the time of enrolment (including first and recurrent cerebral infarctions)
  2. Patients who are 50 years or older
  3. Patients whose neurological signs and symptoms are considered to be stable by the investigator or sub-investigator
  4. Patients with a finding corresponding to the responsible focus confirmed by head X-ray CT or MRI
  5. Patients who have at least two of the following risk factors:

    • diabetes
    • hypertension (systolic blood pressure is 140 mmHg or higher or diastolic blood pressure is 90 mmHg or higher) or under treatment of hypertension
    • smoker (at the time of onset of cerebral infarction)
    • obesity (BMI is more than 25 kg/m2)
    • previous vascular disease (stroke, acute myocardial infarction or peripheral arterial disease before the onset of cerebral infarction)
    • end-organ damage (retinopathy, left ventricular hypertrophy (LVH) or microalbuminuria)
    • hyperlipidaemia

Exclusion Criteria:

  1. Patients with a diagnosis of brain disorders with a bleeding risk such as brain haemorrhage, subarachnoid haemorrhage, cerebral AV malformation, cerebral AV aneurysms and brain tumours
  2. Patients with complications of cardiac disorders (atrial fibrillation, mitral valve stenosis, severe cardiac valve disorders) that may provide an embolic source for cerebral embolism
  3. Patients having had acute coronary syndromes (acute myocardial infarction, unstable angina) within 6 months after enrolment in this study
  4. Patient with hypersensitivity to dipyridamole preparations
  5. Patients with a history of drug allergy to ASA or aspirin asthma
  6. Patients with a history of peptic ulcer
  7. Patients having undergone arterial reconstruction after development of cerebral infarction
  8. Patients with very severe impairment (4 or 5 on Modified Rankin Scale)
  9. Patients with bleeding or bleeding tendencies (haemophilia, haemorrhage urinary tract, vitreous haemorrhage, etc.)
  10. Patients with severe hypertension (systolic blood pressure is 180 mmHg or higher or diastolic blood pressure is 110 mmHg or higher)
  11. Patients with complications such as serious cardiac, renal and hepatic disorders
  12. Patients with a malignant tumour or having had a tumour treatment in the past 5 years
  13. Women who are or may be pregnant or lactating women
Both
50 Years and older
No
 
Japan
 
 
NCT00311402
Boehringer Ingelheim, Study Chair, Boehringer Ingelheim
 
Boehringer Ingelheim Pharmaceuticals
 
Study Chair: Boehringer Ingelheim Boehringer Ingelheim Pharmaceuticals
Boehringer Ingelheim Pharmaceuticals
April 2009

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.