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Antiplatelet Agent
Clopidogrel for Coronary Artery Disease (ISAR-SAFE Trial)
Phase 4
Waitlist Available
Led By Jurriёn M ten Berg, MD
Research Sponsored by Deutsches Herzzentrum Muenchen
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9 months after randomization
Awards & highlights
ISAR-SAFE Trial Summary
The purpose of this study is to determine whether a 6 month duration of clopidogrel therapy after DES implantation is not inferior to that of a 12 month therapy.
ISAR-SAFE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 9 months after randomization
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 months after randomization
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Composite of death, myocardial infarction, stent thrombosis, stroke or TIMI major bleeding.
Secondary outcome measures
The individual components of the primary endpoint
ISAR-SAFE Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: ClopidogrelActive Control1 Intervention
Group II: PlaceboPlacebo Group1 Intervention
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Who is running the clinical trial?
Deutsches Herzzentrum MuenchenLead Sponsor
117 Previous Clinical Trials
83,701 Total Patients Enrolled
27 Trials studying Coronary Artery Disease
29,305 Patients Enrolled for Coronary Artery Disease
Adnan Kastrati, MDStudy ChairDeutsches Herzzentrum Muenchen
32 Previous Clinical Trials
34,069 Total Patients Enrolled
12 Trials studying Coronary Artery Disease
19,230 Patients Enrolled for Coronary Artery Disease
Jurriёn M ten Berg, MDPrincipal InvestigatorSt. Antonius Hospital Nieuwegein, Department of Cardiology
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