NCT Number: NCT00220571
CARESS in Acute Myocardial Infarction
The aim of this study conducted in patients with high risk ST-segment elevation AMI admitted to hospitals with no PTCA facilities is to compare the effects on clinical outcome and cost-effectiveness of two reperfusion strategies:
* Fibrinolytic therapy with Abciximab and half-dose Reteplase, with rescue PTCA in case of lack of reperfusion * Elective referral for "facilitated" PTCA after early administration of Abciximab and half dose of Reteplase
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Notify MeKey information
Conditions
Age range
Up to 75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Cardiologie Hop. Duffaut, Avignon, France
About this study
All patients with ST-segment elevation AMI admitted within 12 hours from symptoms onset will be screened to enter in this study. Data of patients with ST-segment elevation AMI within 12 hours from symptoms onset who do not meet the inclusion criteria or do not sign the informed consent form are entered into a dedicated registry.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- ECG with ST-elevation (≥ 1mm in at least 2 ECG limb leads or ≥ 2 mm in 2 contiguous precordial leads) AMI within <12 hours from symptoms onset fulfilling 1 or more of the following criteria of "high risk":
- Summation of ST-segment elevation or depression ≥ 15 mm in all 12 electrocardiographic leads or new onset complete left bundle branch block;
- Previous myocardial infarction (Q- and non Q-wave);
- Killip Class 2 or 3;
- LV ejection fraction at transthoracic ultrasound < 40%.
Exclusion criteria
- Inability to provide informed consent;
- Age > 75 years
- CABG or PCI procedure in past history involving the infarct-related artery;
- Participation in another study with any investigational drug or device within the previous 30 days;
- Concomitant non-cardiac disease likely to limit long-term prognosis (e.g. cancer);
- Cardiogenic shock (hypotension with Systolic Blood Pressure (SBP) < 90 mmHg and tachycardia > 100 beats / min, not due to hypovolemia and requiring inotropic support or balloon counterpulsation);
- Need for concomitant major surgery (e.g. valve surgery or resection of aortic or left ventricular aneurysm, carotid endarterectomy, abdominal aortic aneurysm surgery, congenital heart disease etc);
- Severe hepatic disease;
- Patients with acute or chronic renal impairment (serum creatinine > 2.0 mg % or 200 mg/l or creatinine clearance < 30 ml/min);
- Transmural MI in different location within the previous week;
- Previous administration of thrombolytics within 7 days;
- Intolerance or contraindications to ASA or Clopidogrel;
- Known leucopenia, defined as a leukocyte count of < 3.500 White Blood Cells (WBC)/ml
- Known neutropenia, defined as < 1000 neutrophils / ml;
- Known thrombocytopenia (< 100.000 platelets / ml );
- Documented active peptic ulcer or upper gastrointestinal bleeding within the previous 6 months;
- Previous hemorrhagic stroke;
- Previous ischemic cerebrovascular event within 3 months;
- Intracranial neoplasm;
- Recent major surgery at risk of bleeding;
- Episodes of uncontrolled hypertension (> 180/110 mmHg despite treatment) in past 2 years;
- Administration of oral anticoagulants within the previous 7 days unless INR ≤ 1.2;
- Severe recent trauma;
- Known or possible pregnancy;
- Absence of suitable vascular access (diffuse peripheral arterial disease);
- Basal ECG changes which make identification of ST-segment elevation impossible (i.e.: ventricular activation from artificial pacemaker, etc.).
Treatment and study plan
Primary outcomes
-
To compare 30 days incidence of the composite end-point of: mortality, reinfarction and refractory ischemia in the two arms of the study.
Time frame: 30 Day
Secondary outcomes
-
Compare 1 year composite end-point of: mortality, reinfarction, refractory ischemia, hospital readmission because of heart failure in the two arms;
Time frame: 1 Year
-
Compare the resource use at 30 days and 1 year, including days in CCU, MICU or general ward, cost of catheterization and PTCA, drugs, ambulance service during index hospitalization and subsequent hospital admissions for reAMI
Time frame: 30 Day and 1 Year
-
Compare the incidence of in-hospital stroke and bleeding complications in the two arms.
Time frame: 30 Day
Interested in participating?
Looking for future studies?
Notify MeSponsors and collaborators
Lead sponsor
Società Italiana di Cardiologia Invasiva
Other
Collaborators
- Biotronik SE & Co. KG
- Eli Lilly and Company
- Royal Brompton & Harefield NHS Foundation Trust
Registry information
Official study title
Combined Abciximab Reteplase Stent Study in Acute Myocardial Infarction
Important dates
- Study start
- 2003
- Study completion
- 2007
- First posted
- Sep 22, 2005
- Registry last updated
- Jul 3, 2007
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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