Aggrenox capsule
Drugextended-release dipyridamole 200 mg plus ASA 50 mg in a capsule, 2 capsules twice daily
NCT Number: NCT00311402
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
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Notify Me50 year and older
All sexes
Interventional
Phase 3
9.178.060 Boehringer Ingelheim Investigational Site, Adachi-ku, Tokyo, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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.
Exclusion criteria
extended-release dipyridamole 200 mg plus ASA 50 mg in a capsule, 2 capsules twice daily
Acetylsalicylic Acid (ASA) 81 mg, 1 tablet once daily
Time frame: Up to 124 weeks
All events reported by investigators were adjudicated by the independent event assessment committee in a blinded manner.
Time frame: Up to 124 weeks
All events reported by investigators were adjudicated by the independent event assessment committee in a blinded manner.
Time frame: Up to 124 weeks
All events reported by investigators were adjudicated by the independent event assessment committee in a blinded manner.
Time frame: Up to 124 weeks
All events reported by investigators were adjudicated by the independent event assessment committee in a blinded manner.
Time frame: Up to 124 weeks
ACS contains acute myocardial infarction (MI), unstable angina and sudden cardiac death. All events reported by investigators were adjudicated by the independent event assessment committee in a blinded manner.
Time frame: Up to 124 weeks
This endpoints were defined as pulmonary embolism, retinal vascular disorder, deep vein thrombosis, peripheral artery obstruction and vascular intervention. All events reported by investigators were adjudicated by the independent event assessment committee in a blinded manner.
Time frame: Up to 124 weeks
This is a composite endpoint of cerebral infarction, transient ischemic attack (TIA), acute myocardial infarction (MI), unstable angina and sudden death attributable to thromboembolism. All events reported by investigators were adjudicated by the independent event assessment committee in a blinded manner.
Boehringer Ingelheim
Industry
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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