NCT03996772CompletedPhase 3
PREvention of STroke in Intracerebral haemorrhaGE Survivors With Atrial Fibrillation
PREvention of STroke in Intracerebral haemorrhaGE Survivors With Atrial Fibrillation (PRESTIGE-AF)
Source: ClinicalTrials.gov · Last updated 13 Jan 2025
Brief summary (registry, in English)
Atrial fibrillation (AF) is the most common form of irregular heart rhythm. In people with AF, blood clots often form in the heart, which can travel to the brain. Blockage of brain arteries by these clots is a major cause of stroke. This type of stroke is called an ischaemic stroke and approximately 15% of all ischaemic strokes are caused by AF. People with AF are often prescribed a medication called an anticoagulant, which makes it less likely for blood clots to form and thus can prevent ischaemic strokes. However, anticoagulants also increase the risk of bleeding, so they are not suitable for everyone. Some people who have AF have had a different type of stroke which is caused by bleeding in the brain, an intracerebral haemorrhage (ICH). These people are at increased risk of suffering both an ischaemic stroke (due to AF) and another ICH. It is not known whether it is best for these people to take an anticoagulant medication or not, as previous research studies did not include this group of people. PREvention of STroke in Intracerebral haemorrhaGE survivors with Atrial Fibrillation (PRESTIGE-AF) is a research study on the best stroke prevention in people with atrial fibrillation (AF) who have recently had a bleeding in their brain, (ICH). This is a trial where half of the participants will take an anticoagulant medication, preventing blood clot formation, and half will not receive an anticoagulant. The direct oral anticoagulants (DOACs) that will be used in this trial are all licenced for use in the United Kingdom and within the European Union (EU) to prevent strokes in people with AF. However, the current licence does not extend to use with people who have had an ICH because it has not been tested in this group with a randomised controlled trial. DOACs will be tested in ICH survivors with AF because previous research trials have shown that people are up to 50% less likely to have bleeding complications in the brain with DOACs than with Warfarin (another commonly used anticoagulant). The aim of PRESTIGE-AF is to answer the question of whether people with ICH and AF should take an anticoagulant medication or if it is better for them to avoid it.
- Status (registry)
- Completed
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 319 (actual)
- First submitted
- 3 Jun 2019
- Start date
- 3 Jun 2019
- Primary completion date
- 31 May 2024
- Lead sponsor
- Imperial College London
- Diseases
- Stroke, Atrial fibrillation
- NCT number
- NCT03996772
- EudraCT number
- 2018-002176-41
What you commit to
- Study type: Interventional · Phase 3
- Participants enrolled: 319
- From 3 Jun 2019 to the primary completion date, 31 May 2024
- 64 sites in 6 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Absolute need for antiplatelet agent (APA) at enrolment, meaning that a patient randomised to receive DOAC who would require an APA is not eligible (single APA is permitted in control group only, at time of randomisation). Presence of a left atrial appendage occlusion device (LAAO) or plan to implant an LAAO
- Participation in any clinical study with an Investigational Medicinal Product within the past 30 days or 5 half-lives of the study drug (observational studies are permitted)
Other illness
- Presence of any medical, psychological, or psychiatric condition which in the opinion of the Principal or Co-Investigator would cause participation in the Study to be unwise
Lab values
- Patient has hypertension, which in the opinion of the investigator, is uncontrollable with medication Any contraindication (except intracerebral haemorrhage) to treatment with apixaban, dabigatran, edoxaban, rivaroxaban as per SmPC. Including any of the following:
- Hypersensitivity to the active principle or any of the excipients
- Clinically relevant bleeding in progress
- Liver disease associated with coagulopathy and a clinically relevant bleeding risk
- Injuries or conditions such as a significant risk of major bleeding
- Hepatic impairment or liver disease which can have an impact on survival
- Exclusion of patients with end-stage renal creatinine clearance CrCL, (CrCL \<15 ml / min) or in patients undergoing dialysis
- Concomitant treatment with other anticoagulants
- Patients with a history of thrombosis and antiphospholipid antibody syndrome Special warnings and precautions for use for apixaban, dabigatran, edoxaban, rivaroxaban as per SmPC should also be taken into account at randomisation.
Other
- Fully dependent (mRS \>4)
- Women who are pregnant, breastfeeding, or plan to become pregnant during the Study period
- Women of childbearing potential (WOCBP see section 12.2 for definition) who are unable or unwilling to take measures for effective contraception (4.9)
- Enrolment occurring before 14 days after the date of ICH
- Enrolment occurring longer than 12 months after the date of ICH
- ICH resulting from trauma or vascular malformation
- Another indication for long-term anticoagulation
Who the study is looking for
- Age ≥ 18 years
- Written informed consent obtained from the patient, or for patients who lack the capacity to consent this can be provided by an appropriate representative as defined in protocol
- Non-traumatic spontaneous ICH during the 12 months before enrolment. Patients become eligible 14 days after the date of their ICH.
- Documented evidence of AF (paroxysmal, persistent or permanent)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (64)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Krankenhaus der Barmherzigen Brüder Eisenstadt Coordinator of this site? Confirm its status | Eisenstadt | Austria | Unknown status |
| Medizinische Universität Graz Coordinator of this site? Confirm its status | Graz | Austria | Unknown status |
| Klinikum Klagenfurt am Worthersee Coordinator of this site? Confirm its status | Klagenfurt | Austria | Unknown status |
| Universitätsklinikum St. Pölten Coordinator of this site? Confirm its status | Sankt Pölten | Austria | Unknown status |
| Universitätsklinikum Aachen Coordinator of this site? Confirm its status | Aachen | Germany | Unknown status |
| Klinikum Altenburger Land Coordinator of this site? Confirm its status | Altenburg | Germany | Unknown status |
| Universitätsklinikum Augsburg Coordinator of this site? Confirm its status | Augsburg | Germany | Unknown status |
| RHÖN-KLINIKUM Campus Bad Neustadt Coordinator of this site? Confirm its status | Bad Neustadt an der Saale | Germany | Unknown status |
| Vivantes Hospital Neukolin Coordinator of this site? Confirm its status | Berlin | Germany | Unknown status |
| Universitätsklinikum Knappschaftskrankenhaus Bochum Coordinator of this site? Confirm its status | Bochum | Germany | Unknown status |
| Knappschaftskrankenhaus Bottrop Coordinator of this site? Confirm its status | Bottrop | Germany | Unknown status |
| University Hospital Cologne Coordinator of this site? Confirm its status | Cologne | Germany | Unknown status |
| Klinikum Dortmund Coordinator of this site? Confirm its status | Dortmund | Germany | Unknown status |
| Technische Universität Dresden Coordinator of this site? Confirm its status | Dresden | Germany | Unknown status |
| Universitätsklinikum Düsseldorf Coordinator of this site? Confirm its status | Düsseldorf | Germany | Unknown status |
| University Hospital Erlangen Coordinator of this site? Confirm its status | Erlangen | Germany | Unknown status |
| Alfried Krupp Von Bohlen und Halbach-Krankenhaus Coordinator of this site? Confirm its status | Essen | Germany | Unknown status |
| University Hospital Frankfurt Coordinator of this site? Confirm its status | Frankfurt | Germany | Unknown status |
| Universitiaetsklinikum Giessen und Marburg (UKGM) - Standort Giessen Coordinator of this site? Confirm its status | Geißen | Germany | Unknown status |
| Bezirkskrankenhaus Günzburg Coordinator of this site? Confirm its status | Günzburg | Germany | Unknown status |
| Medizinische Hochschule Hannover Coordinator of this site? Confirm its status | Hanover | Germany | Unknown status |
| University Hospital Heidelberg Coordinator of this site? Confirm its status | Heidelberg | Germany | Unknown status |
| University of Leipzig Coordinator of this site? Confirm its status | Leipzig | Germany | Unknown status |
| University Hospital Schleswig-Holstein Campus Luebeck Coordinator of this site? Confirm its status | Lübeck | Germany | Unknown status |
| Johannes Wesling Klinikum Minden Coordinator of this site? Confirm its status | Minden | Germany | Unknown status |
| Klinikum der Landeshauptstadt Stuttgart Coordinator of this site? Confirm its status | Stuttgart | Germany | Unknown status |
| Universitätsklinikum Tübingen Coordinator of this site? Confirm its status | Tübingen | Germany | Unknown status |
| Universitätsklinikum Ulm Coordinator of this site? Confirm its status | Ulm | Germany | Unknown status |
| Universitätsklinikum Wuerzburg Coordinator of this site? Confirm its status | Würzburg | Germany | Unknown status |
| Hospital Universitario Torrecárdenas Coordinator of this site? Confirm its status | Almería | Spain | Unknown status |
| Hospital Universitari Vall d'Hebron Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Fundacío Institut d'Investigacío Biomèdica de Bellvitge Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Hospital Germans Trias i Pujol Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Hospital Dr. Josep Trueta Coordinator of this site? Confirm its status | Girona | Spain | Unknown status |
| Hospital Universitario de la Princesa Coordinator of this site? Confirm its status | Madrid | Spain | Unknown status |
| Complejo Hospitalario Universitario de Santiago Coordinator of this site? Confirm its status | Santiago | Spain | Unknown status |
| Hospital Universitario Virgen Macarena Coordinator of this site? Confirm its status | Seville | Spain | Unknown status |
| Hospital Universitario Virgen del Rocio Coordinator of this site? Confirm its status | Seville | Spain | Unknown status |
| Hospital Clínico Universitario de Valladolid Coordinator of this site? Confirm its status | Valladolid | Spain | Unknown status |
| Centre hospitalier Universitaire de Bordeaux Coordinator of this site? Confirm its status | Bordeaux | France | Unknown status |
| Centre Hospitalier Universitaire de Caen Normandie Coordinator of this site? Confirm its status | Caen | France | Unknown status |
| East Kent Hospitals University NHS Foundation Trust Coordinator of this site? Confirm its status | Ashford | United Kingdom | Unknown status |
| Northumbria Healthcare NHS Foundation Trust Coordinator of this site? Confirm its status | Ashington | United Kingdom | Unknown status |
| Basildon and Thurrock University Hospitals NHS Trust Coordinator of this site? Confirm its status | Basildon | United Kingdom | Unknown status |
| Cambridge University Hospitals NHS Trust Coordinator of this site? Confirm its status | Cambridge | United Kingdom | Unknown status |
| Countess of Chester Hospital Coordinator of this site? Confirm its status | Chester | United Kingdom | Unknown status |
| Hull and East Yorkshire NHS Trust Coordinator of this site? Confirm its status | Hull | United Kingdom | Unknown status |
| Kings College Hospital NHS Foundation Trust Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| Imperial College Healthcare NHS Trust Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| St Helens and Knowsley Teaching Hospital NHS Trust Coordinator of this site? Confirm its status | Prescot | United Kingdom | Unknown status |
| Taunton and Somerset NHS Foundation Trust Coordinator of this site? Confirm its status | Taunton | United Kingdom | Unknown status |
| Mid Yorkshire Hospitals NHS Trust Coordinator of this site? Confirm its status | Wakefield | United Kingdom | Unknown status |
| West Hertfordshire Hospitals NHS Trust Coordinator of this site? Confirm its status | Watford | United Kingdom | Unknown status |
| Azienda USL Umbria 1 - Ospedale di Branca-Gubbio Coordinator of this site? Confirm its status | Branca | Italy | Unknown status |
| Ospedale Bufalini di Cesena Coordinator of this site? Confirm its status | Cesena | Italy | Unknown status |
| Azienda USL Umbria 1 - Ospedale di Città di Castello Coordinator of this site? Confirm its status | Città di Castello | Italy | Unknown status |
| Azienda USL Umbria 2 Coordinator of this site? Confirm its status | Foligno | Italy | Unknown status |
| IRCCS Ospedale Policlinico San Martino Coordinator of this site? Confirm its status | Genova | Italy | Unknown status |
| Istituto Clinico Humanitas Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| Azienda Ospedaliera di Rilievo Nazionale (A.O.R.N) A. Cardarelli di Napoli Coordinator of this site? Confirm its status | Naples | Italy | Unknown status |
| Azienda Ospedaliera di Perugia Coordinator of this site? Confirm its status | Perugia | Italy | Unknown status |
| Azienda USL IRCCS di Reggio Emilia Coordinator of this site? Confirm its status | Reggio Emilia | Italy | Unknown status |
| Azienda Ospedaliera S Camillo Forlanini Coordinator of this site? Confirm its status | Rome | Italy | Unknown status |
| Azienda Ospedaliera Universitaria Senese Coordinator of this site? Confirm its status | Siena | Italy | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.