European Registry on STEMI Patients Transferred for PCI With Upstream Use of Abciximab - EuroTransfer Registry
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Purpose
EUROTRANSFER Registry is a prospective, international, web-based European Registry on Patients with ST-Elevation MI Transferred for Mechanical Reperfusion (PCI) with a Special Focus on Upstream Use of Abciximab.
This registry is designed to collect data on approximately 1800 patients during a 12 month enrollment period in up to 20 interventional cardiology centres with hospital transfer networks from all over Europe.
Analysis of this registry should allow to monitor transfer timelines of patients arriving to the cath-lab from the regional hospital with or without upstream start of abciximab and scheduled for mechanical reperfusion (PCI) as well as to monitor regional differences across Europe in regard to the impact that time of various stages of the treatment chain may have on clinical outcomes.
| Condition |
|---|
|
ST-Elevation Myocardial Infarction Acute Coronary Syndrome |
| Study Type: | Observational |
| Study Design: | Observational Model: Defined Population Observational Model: Natural History Time Perspective: Cross-Sectional Time Perspective: Prospective |
| Official Title: | European Registry on Patients With ST-Elevation MI Transferred for Mechanical Reperfusion (PCI)With a Special Focus on Upstream Use of Abciximab |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
PATIENTS:
All consecutive STEMI patients >=18years arriving to the Cath Lab hospital (invasive facility center) from transfer.
Transfer with respect to this registry is defined as patients that reach the Cath Lab hospital:
- transferred from a surrounding regional community hospitals that the Cath Lab hospital has an established referral pattern with or
after being picked–up by an ambulance which is equipped/staffed to provide specific medical therapy (like prehospital thrombolysis or upstream abciximab). Usually these have a physician or specifically trained nurse on board.
CENTRES:
- Provide 24 hour/7 days on duty PCI service.
- Has an established regional hospital referral network with >=8 patients/month arriving from transfer (as defined above).
- A rate of >=10% of these transfer patients who receive upstream abciximab before or during transfer to the Cath Lab hospital. Start of abciximab in the ER or CCU of the Cath Lab hospital will not be considered as upstream start of abciximab.
Exclusion Criteria:
- Patients who arrive to the Cath Lab from other pathways than those specified above (a. and b.), e.g. those who come by ambulances that do not provide specific medical therapy or arrive directly to the ER of the Cath Lab hospital by own feet/car will not be included in this registry.
- Patients from controlled clinical trials shall be included as long as their actual treatment is fully known. Thus, participants from randomized trials with blinded treatment cannot be included in this registry.
Contacts and Locations| Finland | |
| Helsinki University Central Hospital | |
| Helsinki, Finland | |
| Germany | |
| Schwarzwald-Baar Klinikum Villingen-Schwenningen GmbH | |
| Villingen, Germany | |
| Italy | |
| San Donato Hospital | |
| Arezzo, Italy | |
| Ospedale Carlo Poma | |
| Mantova, Italy | |
| Ospedale G.Pasquinucci | |
| Massa, Italy | |
| Santa Maria Nuova Hospital Reggio Emilia | |
| Reggio Emilia, Italy | |
| Ospedale S.Maria di Ca Foncello | |
| Treviso, Italy | |
| Poland | |
| Cardiac Catheterization Laboratories Jagiellonian University Medical College, University Hospital | |
| Krakow, Poland, 31-501 | |
| Department of Interventional Cardiology, John Paul II Hospital | |
| Krakow, Poland | |
| Szpital Wojewodzki w Przemyslu | |
| Przemysl, Poland | |
| Szpital im. Szczeklika Tarnow | |
| Tarnow, Poland | |
| Slovenia | |
| University Medical Center Ljubljana | |
| Ljubljana, Slovenia | |
| Spain | |
| Hospital Juan Canalejo | |
| Coruna, Spain | |
| Hospital Clinico Universitario | |
| Santiago de Compostela, Spain | |
| Sweden | |
| Linköping University Hospital | |
| Linköping, Sweden | |
| Principal Investigator: | Dariusz Dudek, Assoc. Prof. | Cardiac Catheterization Laboratories, Jagiellonian University Medical College |
| Study Chair: | Zbigniew Siudak, MD | Cardiac Catheterization Laboratories, Jagiellonian University Medical College |
| Study Director: | Lukasz Partyka, MD, PhD | Krakow Cardiovascular Research Institute |
More Information
Additional Information:
No publications provided by Jagiellonian University
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00378391 History of Changes |
| Other Study ID Numbers: | H4S-PL-O067 |
| Study First Received: | September 19, 2006 |
| Last Updated: | June 19, 2007 |
| Health Authority: | Poland: Ministry of Health |
Keywords provided by Jagiellonian University:
|
ST-Elevation Myocardial Infarction upstream abciximab guideline adherence hospital networking |
Additional relevant MeSH terms:
|
Infarction Myocardial Infarction Acute Coronary Syndrome Ischemia Pathologic Processes Necrosis Myocardial Ischemia Heart Diseases Cardiovascular Diseases Vascular Diseases |
Angina Pectoris Chest Pain Pain Signs and Symptoms Abciximab Platelet Aggregation Inhibitors Hematologic Agents Therapeutic Uses Pharmacologic Actions Anticoagulants |
ClinicalTrials.gov processed this record on May 16, 2013