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Patients admitted to hospital with chest pain due to reduced blood flow to heart muscle (diagnosis Acute Coronary Syndrome) can be treated with medication and an angioplasty ± stent procedure, which restores blood flow to the heart. Antiplatelet drugs (Aspirin and Clopidogrel) are blood thinning treatments and research has reported they reduce heart attacks, death and stroke. The investigators know some patients do not respond fully to Clopidogrel but currently patients are not tested for this.
The investigators wish to perform a trial to identify those patients who do not respond fully to Clopidogrel and randomise them to either Prasugrel (newer drug) or a higher dose of Clopidogrel.
Patients admitted to the hospitals (2 in the UK and 1 in Germany) will be asked for their consent to participate. A blood sample is tested for platelet activity.
Full description
STUDY DESCRIPTION This is a multinational, randomised open label study comparing Prasugrel versus Clopidogrel in ACS patients who have high platelet reactivity managed with an early invasive strategy (PCI as early as possible and no later than 72 hours from admission).
Patients identified with low platelet reactivity indicating a good response to Clopidogrel will be entered into an observational Registry.
Sites There will be three participating hospitals, two in the UK and one in Germany.
Screening All patients admitted to the hospital with suspected ACS requiring early PCI (within 3 days of admission) will be screened for entry into the trial.
The investigator and/or his/her designee will explain the study requirements and procedures and obtain consent before any study procedures are performed.
We estimate approximately 500 patients will be screened. From these a total of 140 patients will be randomised, the remaining screened patients will be entered into the registry. There will be competitive recruitment and each site is expected to randomise about 40 to 50 patients each. We estimate 7 to 8 patients randomised per month over a period of 18 months.
Routine blood tests and investigations will be carried out according to local management strategies. The angiogram and PCI procedure are part of the routine management for this patient and will be performed according to local policies and procedures.
A research blood sample will be required to determine platelet activity which has to be taken > 2hours from the standard Clopidogrel pre-PCI loading. For most patients this will be taken in the catheter laboratory around the PCI procedure. In a few patients who are loaded with Clopidogrel close to the PCI procedure the blood samples may be taken in the ward or recovery area. Depending on the platelet activity results patients will be either entered into the registry or randomly allocated to either Clopidogrel or Prasugrel.
REGISTRY PATIENTS Patients will continue on the standard treatment of Clopidogrel. Data will be collected of routine blood tests and investigations, medication and procedures. Additional blood samples will be taken (if patient consents) for the biomarker and genetic sub-studies. Their GP will be contacted at 30±5 days to see if they are alive.
RANDOMISED PATIENTS Randomisation Investigators will access an automated telephone or automated web service. Investigators will have to confirm patient fulfils the eligibility criteria and that consent has been obtained.
Randomised Treatment Randomised patients will be allocated to receive either open label Clopidogrel (Plavix) or Prasugrel (Efient).
Group 1: Clopidogrel (Plavix)
Group 2: Prasugrel (Efient)
Drug Supply and Storage Prasugrel, a commercially available product, will be supplied by Eli Lilly which holds the manufacturing license to produce Prasugrel. Clopidogrel (Plavix) will be purchased by the hospital Pharmacy through normal purchasing arrangements. All study drugs should be stored in an appropriate locked room, under the control of the Hospital Pharmacist or the Investigator, in the conditions described in the package insert.
Hospital Admission to Discharge
One Month Follow UP RCT Patients in the RCT will be required to attend the hospital for a follow up visit at 30±5 days from date of randomisation. Patients will be assessed by the investigator or his/her designee for heart rate and blood pressure, medication tolerance and compliance, occurrence of adverse events and clinical endpoints, blood sample for platelet activity. At this time the investigator will discuss with the patient their treatment options after this period.
Sub-studies There are two sub-studies proposed (i) biomarker and (ii) genetic. Blood samples will be taken and stored locally before shipment to a core lab in Germany.
Enrollment
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Inclusion criteria
Exclusion criteria
Patients <18 years and >75 years
Body weight <60kg
Pretreatment with prasugrel within 7 days of randomisation
History of stroke or transient ischaemic attack
Patients with increased bleeding risk e.g.
Hb<10g/dL
Intracranial neoplasm, arteriovenous malformation or aneurysm.
Severe hepatic impairment (Child Pugh class C)
Intention to use the following medications
Female patients who are pregnant, planning pregnancy, not using reliable contraception or who are breastfeeding
Known allergy, hypersensitivity or other contraindications to prasugrel or clopidogrel
Primary purpose
Allocation
Interventional model
Masking
44 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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