Doctors track bleeding risks in 1,000+ heart attack patients
NCT ID NCT04471870
Summary
This study observed over 1,000 heart attack patients who received a specific intravenous blood thinner (cangrelor) during a procedure to open blocked heart arteries. Researchers tracked patients for 30 days as they switched from the IV medication to common oral blood thinners. The main goal was to collect real-world safety information, specifically monitoring for bleeding complications and major heart-related problems.
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Contacts and locations
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Locations
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A.O. Mauriziano
Torino, Italy
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A.O. Padova
Padua, Italy
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A.O. Sant'Anna e San Sebastiano
Caserta, Italy
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A.O.R.N. A. Cardarelli
Naples, Italy
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A.O.U. Careggi
Florence, Italy
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A.O.U. Consorziale Policlinico
Bari, Italy
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A.O.U. Federico II
Naples, Italy
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A.O.U. Policlinico-Vittorio Emanuele P.O. Ferrarotto
Catania, Italy
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A.O.U. Riuniti
Ancona, Italy
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A.O.U. Sassari
Sassari, Italy
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ASO Santa Croce e Carle
Cuneo, Italy
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Aurelia Hospital
Roma, Italy
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Azienda Ospedaliera San Pio
Benevento, Italy
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Centro Cardiologico Monzino
Milan, Italy
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Fondazione Poliambulanza
Brescia, Italy
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Fondazione Policlinico Universitario A. Gemelli
Roma, Italy
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Fondazione Toscana "G. Monasterio" Ospedale del Cuore G. Pasquinucci
Massa, Italy
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Ospedale Ca' Foncello
Treviso, Italy
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Ospedale Fabrizio Spaziani
Frosinone, Italy
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Ospedale Maggiore
Bologna, Italy
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Ospedale S. Andrea
La Spezia, Italy
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Ospedale SS Annunziata
Cosenza, Italy
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Ospedale San Bassiano
Bassano del Grappa, Italy
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Ospedale San Donato
Arezzo, Italy
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Ospedale Santa Chiara
Trento, Italy
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Ospedale Santa Maria Goretti
Latina, Italy
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Ospedale Umberto I
Syracuse, Italy
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Ospedale degli Infermi
Rivoli, Italy
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Policlinico San Matteo
Pavia, Italy
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San Camillo Forlanini
Roma, 00152, Italy
Conditions
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