EUCTR2011-001686-40-DEActive, not recruitingNot Applicable
INTRACORONARY STENTING AND ANTITHROMBOTIC REGIMEN: ADJUSTING ANTIPLATELET TREATMENT IN PATIENTS BASED ON PLATELET FUNCTION TESTING - ISAR ADAPT-PF - ISAR ADAPT-PF
German Heart Centre Munich, Department of Cardiovascular Diseases0 sites70 target enrollmentStarted: June 6, 2011Last updated:
Conditions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 70
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •- patients after coronary intervention
- •- insufficient inhibition of platelet aggregation after Clopidogrel loading
- •- informed, written consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 35
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 35
Exclusion Criteria
- •- age < 18 years >, > 80 years
- •- body weight < 60 kg
- •- surgical intervention < 6 weeks
- •- apoplexy in anamnesis
- •- cardiogenic shock
- •- oral anticoagulation
- •- GPIIb/IIIa antagonists < 10 days or periprocedural
- •- platelet count < 100.000/µl
- •- increased risk for bradycardia
- •- severe liver dysfunction
- •- dialysis-dependent renal insufficiency
- •- simultaneous taking of CYP3A4 inhibitors
Investigators
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