Coronary Heart Disease Clinical Trial
Official title:
Influence Of Omeprazole On The Anti-Platelet Action Of Clopidogrel Associated To Aspirin: Double-Blind Randomized Trial Against Placebo
Objectives: A prospective investigation of the effect of omeprazole, a proton pump
inhibitor, on the anti-platelet action of clopidogrel.
The main decision criterion will concern change in VASP protein phosphorylation under
treatment. Phosphorylation will be measured before and after administration of omeprazole
versus placebo in patients undergoing clopidogrel treatment.
Type of study: Single center, double blind, randomized parallel group study versus placebo,
comparing two treatment groups:
- clopidogrel + omeprazole + standard regime (beta-blockers, atorvastatin, IEC, aspirin)
- clopidogrel + placebo+ standard regime (beta-blockers, atorvastatin, IEC, aspirin)
Study population: 120 patients from the Cardiology Department of Brest University hospital,
Brest (France), receiving a standard treatment comprising a loading dose of clopidogrel
followed by a daily dose of 75 mg associated to 75 mg aspirin, will be randomized between 20
mg/day omeprazole and 20 mg/day placebo treatment groups. The efficacy of clopidogrel will
be assessed by inter-group comparison on the VASP test.
Study period: 7 days' treatment per patient. Total study period estimated at 6 months.
Expected findings: The results should confirm the suspected negative effect of omeprazole on
clopidogrel's impact on arterial thrombosis risk, secondarily allowing new recommendations
to be drawn up for this association.
Preventing recurrence of thrombosis following angioplasty relies on dual-therapy associating
the anti-platelet agents aspirin and clopidogrel. This regime is kept up for between 1 and 6
months, depending on the type of stent deployed in the angioplasty. The biological
effectiveness of the clopidogrel treatment can be assessed by the VASP test, a new platelet
test, results on which have been shown to correlate with risk of thrombosis. A study we ran
recently strongly suggested that omeprazole was associated with a poor response to
clopidogrel. Omeprazole is an anti-ulcer agent frequently prescribed to prevent unwanted
side-effects of aspirin, making it frequently associated to clopidogrel in the aftermath of
angioplasty.
Study population: 120 patients from the Cardiology Department of Brest University hospital,
Brest (France), receiving a standard treatment comprising a loading dose of clopidogrel
followed by a daily dose of 75 mg associated to 75 mg aspirin, will be randomized between 20
mg/day omeprazole and 20 mg/day placebo treatment groups. The efficacy of clopidogrel will
be assessed by inter-group comparison on the VASP test.
Study period: 7 days' treatment per patient. Total study period estimated at 6 months.
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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