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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
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

Full criteria on ClinicalTrials.gov

Sites (64)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Krankenhaus der Barmherzigen Brüder Eisenstadt
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EisenstadtAustriaUnknown status
Medizinische Universität Graz
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GrazAustriaUnknown status
Klinikum Klagenfurt am Worthersee
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KlagenfurtAustriaUnknown status
Universitätsklinikum St. Pölten
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Sankt PöltenAustriaUnknown status
Universitätsklinikum Aachen
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AachenGermanyUnknown status
Klinikum Altenburger Land
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AltenburgGermanyUnknown status
Universitätsklinikum Augsburg
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AugsburgGermanyUnknown status
RHÖN-KLINIKUM Campus Bad Neustadt
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Bad Neustadt an der SaaleGermanyUnknown status
Vivantes Hospital Neukolin
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BerlinGermanyUnknown status
Universitätsklinikum Knappschaftskrankenhaus Bochum
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BochumGermanyUnknown status
Knappschaftskrankenhaus Bottrop
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BottropGermanyUnknown status
University Hospital Cologne
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CologneGermanyUnknown status
Klinikum Dortmund
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DortmundGermanyUnknown status
Technische Universität Dresden
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DresdenGermanyUnknown status
Universitätsklinikum Düsseldorf
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DüsseldorfGermanyUnknown status
University Hospital Erlangen
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ErlangenGermanyUnknown status
Alfried Krupp Von Bohlen und Halbach-Krankenhaus
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EssenGermanyUnknown status
University Hospital Frankfurt
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FrankfurtGermanyUnknown status
Universitiaetsklinikum Giessen und Marburg (UKGM) - Standort Giessen
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GeißenGermanyUnknown status
Bezirkskrankenhaus Günzburg
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GünzburgGermanyUnknown status
Medizinische Hochschule Hannover
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HanoverGermanyUnknown status
University Hospital Heidelberg
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HeidelbergGermanyUnknown status
University of Leipzig
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LeipzigGermanyUnknown status
University Hospital Schleswig-Holstein Campus Luebeck
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LübeckGermanyUnknown status
Johannes Wesling Klinikum Minden
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MindenGermanyUnknown status
Klinikum der Landeshauptstadt Stuttgart
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StuttgartGermanyUnknown status
Universitätsklinikum Tübingen
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TübingenGermanyUnknown status
Universitätsklinikum Ulm
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UlmGermanyUnknown status
Universitätsklinikum Wuerzburg
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WürzburgGermanyUnknown status
Hospital Universitario Torrecárdenas
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AlmeríaSpainUnknown status
Hospital Universitari Vall d'Hebron
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BarcelonaSpainUnknown status
Fundacío Institut d'Investigacío Biomèdica de Bellvitge
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BarcelonaSpainUnknown status
Hospital Germans Trias i Pujol
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BarcelonaSpainUnknown status
Hospital Dr. Josep Trueta
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GironaSpainUnknown status
Hospital Universitario de la Princesa
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MadridSpainUnknown status
Complejo Hospitalario Universitario de Santiago
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SantiagoSpainUnknown status
Hospital Universitario Virgen Macarena
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SevilleSpainUnknown status
Hospital Universitario Virgen del Rocio
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SevilleSpainUnknown status
Hospital Clínico Universitario de Valladolid
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ValladolidSpainUnknown status
Centre hospitalier Universitaire de Bordeaux
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BordeauxFranceUnknown status
Centre Hospitalier Universitaire de Caen Normandie
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CaenFranceUnknown status
East Kent Hospitals University NHS Foundation Trust
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AshfordUnited KingdomUnknown status
Northumbria Healthcare NHS Foundation Trust
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AshingtonUnited KingdomUnknown status
Basildon and Thurrock University Hospitals NHS Trust
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BasildonUnited KingdomUnknown status
Cambridge University Hospitals NHS Trust
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CambridgeUnited KingdomUnknown status
Countess of Chester Hospital
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ChesterUnited KingdomUnknown status
Hull and East Yorkshire NHS Trust
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HullUnited KingdomUnknown status
Kings College Hospital NHS Foundation Trust
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LondonUnited KingdomUnknown status
Imperial College Healthcare NHS Trust
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LondonUnited KingdomUnknown status
St Helens and Knowsley Teaching Hospital NHS Trust
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PrescotUnited KingdomUnknown status
Taunton and Somerset NHS Foundation Trust
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TauntonUnited KingdomUnknown status
Mid Yorkshire Hospitals NHS Trust
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WakefieldUnited KingdomUnknown status
West Hertfordshire Hospitals NHS Trust
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WatfordUnited KingdomUnknown status
Azienda USL Umbria 1 - Ospedale di Branca-Gubbio
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BrancaItalyUnknown status
Ospedale Bufalini di Cesena
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CesenaItalyUnknown status
Azienda USL Umbria 1 - Ospedale di Città di Castello
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Città di CastelloItalyUnknown status
Azienda USL Umbria 2
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FolignoItalyUnknown status
IRCCS Ospedale Policlinico San Martino
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GenovaItalyUnknown status
Istituto Clinico Humanitas
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MilanItalyUnknown status
Azienda Ospedaliera di Rilievo Nazionale (A.O.R.N) A. Cardarelli di Napoli
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NaplesItalyUnknown status
Azienda Ospedaliera di Perugia
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PerugiaItalyUnknown status
Azienda USL IRCCS di Reggio Emilia
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Reggio EmiliaItalyUnknown status
Azienda Ospedaliera S Camillo Forlanini
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RomeItalyUnknown status
Azienda Ospedaliera Universitaria Senese
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SienaItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.