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RECRUITING
NCT06823466

Advancing Knowledge in Ischemic Stroke Patients on Oral Anticoagulants

Sponsor: University of L'Aquila

View on ClinicalTrials.gov

Summary

The Advancing knowledge in ischemic Stroke PatiEnts on oRal Anticoagulants (ASPERA) study aims to investigate characteristics of ischemic stroke cases occurring in patients on oral anticoagulation for atrial fibrillation (AF) or other cardioembolic arrhythmias and to characterize short and long-term outcomes associated with different secondary prevention strategies to prevent stroke recurrences. The ASPERA study is a multicenter, observational, both retrospective and prospective real-world study involving acute ischemic stroke patients occurring on oral anticoagulation. The study will encompass a retrospective (ASPERA-R) and prospective (ASPERA-P) data collection. Patient will be recruited consecutively at different emergency services and stroke units worldwide. University of L'Aquila (UnivAQ) will be in charge of study coordination, data analysis and management. The duration of ASPERA-R will be of 5-year from the study initiation of the study. Participating centers will be given a 6-month timeframe to enter retrospective data, commencing from the date of study approval. ASPERA-P duration will be of 2 years of enrollment from the study approval and follow-up of 5 years. (study conclusion after 7 years of approval). Inclusion criteria will be: 1.Confirmed diagnosis of ischemic stroke. 2. Availability of at least one neuroimaging exam positive for ischemic lesion(s) consistent with patient symptoms. 3. Ongoing oral anticoagulation at the time of the index ischemic stroke. 4. Prior diagnosis of atrial fibrillation or other cardioembolic arrhythmias. 5. Written informed consent provided by the patient himself or by proxy. Patients with Symptoms not indicative of acute stroke, ongoing intravenous or subcutaneous anticoagulation at the time of stroke will be excluded. ASPERA-R: characterization of demographic, clinical and neuroimaging features of ischemic stroke cases occurring on oral anticoagulants. The primary outcome will be: ASPERA-R : characterization of demographic, clinical and neuroimaging features of ischemic stroke cases occurring on oral anticoagulants. ASPERA-P: risk of ischemic stroke recurrence of ischemic stroke cases occurring on oral anticoagulants across different secondary preventive strategies (i.e., maintaining the same type of oral anticoagulation versus switching to a different secondary prevention strategy) at 90 days, 1 and 5 years after the index stroke. Additionally, the study will aim to investigate the risk of safety events (hemorrhagic transformation, intracranial hemorrhage, other major bleeding events, any bleeding events, death due to any cause), risk of other major ischemic events (transient ischemic attack, myocardial infarction, death due to vascular causes) at each follow-up and to identify demographic, clinical and neuroimaging features of ischemic stroke recurrences.

Official title: Advancing Knowledge in Ischemic Stroke Patients on Oral Anticoagulants - The ASPERA International Registry

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2025-02-12

Completion Date

2031-02-12

Last Updated

2025-02-20

Healthy Volunteers

No

Locations (47)

Department of Neurology, Sveti Duh University Hospital

Zagreb, Croatia

Copenhagen University Hospital, Bispebjerg Hospital

Copenhagen, Denmark

Neurology Department, Assiut University Hospitals

Asyut, Egypt

Neurology Department, Faculty of Medicine , Ain Shams University

Cairo, Egypt

Neurology Unit, Kobry Elkoba Medical Complex

Cairo, Egypt

Université Cote d'Azur UR2CA-URRIS, Unité Neurovasculaire, CHU Hôpital Pasteur 2

Nice, France

Department of Neurology, Charite, Berlin Germany and Center for Stroke Research (CSB)

Berlin, Germany

Department of Neurology, Martin-Luther-University of Halle-Wittenberg

Halle, Germany

Neurological Clinic, Marche Polytechnic University

Ancona, Italy

SC Neurologia, Stroke Unit, Ospedale di Venere

Bari, Italy

IRCCS Istituto delle Scienze Neurologiche

Bologna, Italy

SCA Neurologia, USL Umbria 1

Città di Castello, Italy

Azienda Ospedaliero-Universitaria di Ferrara, Arcispedale Sant'Anna

Ferrara, Italy

SOD Stroke Unit, Azienda Ospedaliero Universitaria Careggi

Florence, Italy

Stroke Unit, Hospital Fabrizio Spazian

Frosinone, Italy

University of L'Aquila

L’Aquila, Italy

Neurology and Stroke Unit, ASST Grande Ospedale Metropolitano Niguarda

Milan, Italy

Neurology and Stroke Unit, AORN Antonio Cardarelli

Naples, Italy

UOC Neurologia e Stroke Unit, AOOR. Villa Sofia - Cervello

Palermo, Italy

Department of Medicine and Surgery, University of Parma

Parma, Italy

Department of Emergency Neurology and Stroke Unit, IRCCS C. Mondino

Pavia, Italy

Medicina Interna e d'Urgenza - Stroke Unit, Azienda Ospedaliera di Perugia

Perugia, Italy

Department of Emergency Neurology and Stroke Unit, Pescara Hospital

Pescara, Italy

Department of Neuroscience, Neurology Unit, S.Maria delle Croci Hospital, AUSL Romagna

Ravenna, Italy

Neurology Unit, Stroke Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia

Reggio Emilia, Italy

UOSD Stroke Unit, Azienda Ospedaliera San Camillo Forlanini

Rome, Italy

Fondazione Policlinico Universitario Agostino Gemelli

Rome, Italy

UOC Neurologia, Ospedale Provinciale "Madonna del Soccorso"

San Benedetto del Tronto, Italy

UOC Stroke Unit, Emergency and Urgency Department, AOU Senese

Siena, Italy

ASL Abruzzo 4, G.Mazzini Hospital

Teramo, Italy

SOSD Stroke Unit, Department of Head, Neck, and Neuroscience, Udine University Hospital

Udine, Italy

Stroke Unit, Neurologia A, Azienda Ospedaliera Universitaria Integrata di Verona

Verona, Italy

University Clinic of Neurology, University "Ss.Cyril and Methodius"-Faculty of Medicine

Skopje, North Macedonia

Department of Neurology, Jagiellonian University Medical College

Krakow, Poland

Lisbon Central University Hospital - ULS São José and Faculdade de Medicina, Universidade de Lisboa

Lisbon, Portugal

Hospital de Santa Maria

Lisbon, Portugal

Elias University Emergency Hospital, Carol Davila University of Medicine and Pharmacy

Bucharest, Romania

King Abdulaziz Medical City

Riyadh, Saudi Arabia

Vascular Neurology Division National Neuroscience Institute King Fahad Medical City

Riyadh, Saudi Arabia

Department of Neurology, Faculty of Medicine, P. J. Safarik University and University Hospital L. Pasteur

Košice, Slovakia

La Paz University Hospital, Universidad Autónoma de Madrid, IdiPAZ Research Institute

Madrid, Spain

Department of Medicine, University of Valladolid

Valladolid, Spain

University Teaching Hospital St. Gallen

Sankt Gallen, Switzerland

Southmead Hospital, North Bristol NHS Trust

Bristol, UK, United Kingdom

St George's University Hospitals NHS Foundation Trust

London, UK, United Kingdom

Department of Brain Sciences, Imperial College London

London, UK, United Kingdom

Department of Stroke and Neuroscience, Charing Cross Hospital, Imperial College

London, UK, United Kingdom