PRESTIGE-AF: PREvention of STroke in Intracerebral haemorrhaGE Survivors With Atrial Fibrillation

Sponsor

Imperial College London (Other)

Overall Status

Recruiting

CT.gov ID

NCT03996772

Collaborator

Wuerzburg University Hospital (Other), Julius-Maximilians University (Other), Medical University of Graz (Other), University of Birmingham (Other), King's College London (Other), Hospital Universitari Vall d'Hebron Research Institute (Other), University of Bordeaux (Other), Azienda Ospedaliera di Perugia (Other), Aalborg University (Other), STROKE ALLIANCE FOR EUROPE (Other), University Hospital Heidelberg (Other), Cambridge University Hospitals NHS Foundation Trust (Other), Imperial College Healthcare NHS Trust (Other), Mid Yorkshire Hospitals NHS Trust (Other), Hull University Teaching Hospitals NHS Trust (Other), Mid and South Essex NHS Foundation Trust (Other), University Hospital Plymouth NHS Trust (Other), King's College Hospital NHS Trust (Other), East Kent Hospitals University NHS Foundation Trust (Other), Northumbria Healthcare NHS Foundation Trust (Other), West Hertfordshire Hospitals NHS Trust (Other), St Helens & Knowsley Teaching Hospitals NHS Trust (Other), Somerset NHS Foundation Trust (Other), Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (Other), Germans Trias i Pujol Hospital (Other), Royal Free Hospital NHS Foundation Trust (Other), University Hospital Erlangen (Other), Vivantes Netzwerk für Gesundheit GmbH (Other), University of Leipzig (Other), Johannes Wesling Klinikum Minden (Other), University Hospital Frankfurt (Other), Klinikum Altenburger Land (Other), Hannover Medical School (Other), University Hospital Schleswig-Holstein (Other), University Hospital of Cologne (Other), Alfried Krupp Krankenhaus (Other)

654

Enrollment

Locations

Arms

41.9

Anticipated Duration (Months)

23.4

Patients Per Site

0.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Atrial Fibrillation Intracerebral Hemorrhage	Drug: Apixaban Oral Tablet Drug: Dabigatran Drug: Edoxaban Tablets Drug: Rivaroxaban	Phase 3

Detailed Description

Stroke is one of the largest public health challenges worldwide. Its societal impact is expected to further increase in the coming decades due to the aging of population. Importantly, stroke is a heterogeneous disease comprising various subtypes with distinct mechanisms. The variability of individual risks demands that more specifically targeted and better personalised approaches are developed to tailor stroke prevention for particular stroke types and individual patients.

Intracerebral haemorrhage (ICH) is a particularly severe type of stroke affecting 10-15% of all stroke patients. Importantly, ICH carries even higher mortality and more severe disability than other stroke types. While mechanisms of ICH and ischaemic stroke are distinct, many risk factors are shared and patients are often at increased risk of both ischaemic stroke and ICH.

Atrial fibrillation (AF) is also a growing epidemic in aging populations and a major cause of ischaemic stroke due to thrombus formation in the heart migrating to and occluding intracerebral arteries. At least 20% of ICH survivors also suffer from AF and are, thus, at particularly high risk of ischaemic stroke. While ischaemic stroke in AF patients in general can be much more effectively prevented with oral anticoagulation than with antiplatelet agents (APA) concerns about ICH recurrence in ICH survivors are a major barrier for anticoagulation. The best approach to stroke prevention in ICH patients with AF is presently unknown. Current clinical guidelines, which are largely based on retrospective observational studies investigating anticoagulation with vitamin K antagonists (VKA), either recommend considering anticoagulation only in patients with non-lobar location of ICH or, in the absence of evidence from randomised controlled trials, refrain from making any recommendations at all. Anticoagulation with direct oral anticoagulants (DOAC) has proven efficacy and safety for stroke prevention in AF. DOACs may be a better alternative to VKA particularly in ICH patients because DOACs were associated with a 50% lower risk of ICH than VKA in previous clinical trials of stroke prevention in AF. However, patients with previous ICH were excluded from these trials.

Although thousands of ICH survivors with AF every year worldwide need effective prevention of another stroke, the best antithrombotic therapy for these patients is currently unknown. PRESTIGE-AF will be the first sufficiently powered randomised controlled trial aiming to resolve the dilemma of stroke prevention in this challenging high-risk patient population. Specifically, it will answer the question whether DOAC with their well-documented lower risk of intracranial haemorrhagic complications, compared to VKA, provide both a more effective and an equally safe option for stroke prevention in patients with ICH and AF compared to no anticoagulant. Findings of the Study are expected to change management guidelines and future prevention research for ICH survivors with AF.

PREvention of STroke in Intracerebral haemorrhaGE survivors (PRESTIGE-AF) will test whether preventive therapy with DOACs (intervention group) reduce the rate of ischaemic stroke (superiority) compared to no anticoagulation (control group) without unacceptably increasing the risk of recurrent ICH (non-inferiority) in patients with AF and a previous ICH within 6 months before enrolment.

The Research Question is:

Does preventive therapy with Direct Oral Anticoagulants (intervention group) reduce the rate of ischaemic stroke (superiority) compared to no anticoagulation (control group) without unacceptably increasing the risk of recurrent Intracerebral haemorrhage (non-inferiority) in patients with atrial fibrillation and a previous intracerebral haemorrhage within 6 months before enrolment.

The Objectives of the study are:

The main objective is to perform a randomised controlled trial to resolve the long-standing management dilemma of antithrombotic stroke prevention in intracerebral haemorrhage (ICH) survivors with comorbid atrial fibrillation (AF). Specifically, it will address the question whether direct oral anticoagulants (DOACs, intervention) provide a more effective option for prevention of ischaemic stroke and an equally safe option in terms of recurrence of ICH for antithrombotic stroke prevention in survivors of recent ICH compared to no anticoagulation (i.e. no antithrombotic therapy or antiplatelet therapy at Principal Investigator´s discretion).

The secondary Study objectives are:

To examine the effect of anticoagulation with DOAC versus no anticoagulation on major cardiovascular outcomes and mortality in ICH patient with AF
To compare the effect of DOACs versus no anticoagulation on major systemic and intracranial bleeding in this Study population
To examine the effect of DOACs versus no anticoagulation on net clinical benefit in ICH patients with AF

The exploratory objectives are:

• To explore the impact of DOAC vs. no anticoagulation on quality of life, cognition and psychological morbidity in patients with ICH and AF over time Study Design: PRESTIGE-AF is a phase 3b investigator-led, multicentre, parallel group, prospective randomised, open, blinded end-point assessment (PROBE) clinical trial comparing DOACs (interventional arm) against no anticoagulation (control arm) in patients with a recent ICH and comorbid AF.

Randomisation will occur in a 1:1 ratio. Participants will be stratified according to two factors: lobar and non-lobar location of ICH and sex. Choice and dose of DOAC treatment as well as the use of concomitant medication during the study treatment will be at the Principal Investigator´s discretion within the spectrum of licensed doses labelled for stroke prevention in AF patients in Europe following the Summary of Product Characteristics (SmPC). The control group will receive no anticoagulant but the use of an antiplatelet agent is at the Principal Investigator´s discretion who will use their clinical judgment to initiate (or not) an antiplatelet drug of their choice.

Baseline assessment will include capturing Participant's demographics, clinical characteristics, vital signs, medical history, and concomitant diseases as well as documentation of AF (previous history or newly detected). Results of routine diagnostic tests before Study enrolment will be also collected using an electronic case report form. The routine brain imaging data performed after the ICH and before Study enrolment will also be collected at baseline.

After randomisation, Participants will be followed-up in person at various time points (1, 6, 12, 24, 36 months) for up to 3 years. At each visit, outcome events and adverse events will be captured.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

654 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

PREvention of STroke in Intracerebral haemorrhaGE survivors with Atrial Fibrillation is a phase 3b investigator-led, multicentre, parallel group, prospective randomised, open, blinded end-point assessment (PROBE) clinical trial comparing direct oral anticoagulants against no anticoagulation in patients with a recent intracerebral haemorrhage (ICH) and comorbid atrial fibrillation (AF). Randomisation will occur in a 1:1 ratio. Participants will be stratified according to two factors: lobar and non-lobar location of ICH and gender. Choice and dose of direct oral anticoagulant treatment and use of concomitant medication during the study treatment will be at the Principal Investigator´s discretion within the licensed doses for stroke prevention in AF patients in Europe. The control group will receive no anticoagulant but the use of an antiplatelet is at the Principal Investigator´s discretion who will use their clinical judgment to initiate an antiplatelet drug of their choice.PREvention of STroke in Intracerebral haemorrhaGE survivors with Atrial Fibrillation is a phase 3b investigator-led, multicentre, parallel group, prospective randomised, open, blinded end-point assessment (PROBE) clinical trial comparing direct oral anticoagulants against no anticoagulation in patients with a recent intracerebral haemorrhage (ICH) and comorbid atrial fibrillation (AF). Randomisation will occur in a 1:1 ratio. Participants will be stratified according to two factors: lobar and non-lobar location of ICH and gender. Choice and dose of direct oral anticoagulant treatment and use of concomitant medication during the study treatment will be at the Principal Investigator´s discretion within the licensed doses for stroke prevention in AF patients in Europe. The control group will receive no anticoagulant but the use of an antiplatelet is at the Principal Investigator´s discretion who will use their clinical judgment to initiate an antiplatelet drug of their choice.

Masking:

Single (Outcomes Assessor)

Masking Description:

An Event Adjudication Committee (EAC) will be established. The EAC will consist of experts in relevant fields of the Study such as neurology, cardiology, and haematology. An event adjudication charter with clear definitions of pre-specified outcome events will be developed by the steering committee and agreed by the EAC. After formal training, the EAC will be provided with pseudonymised data for adjudication of pre-specified outcome events and serious adverse events using an online platform provided by the data management centre, Clinical Trials Center Wuerzburg at the University of Wuerzburg.

Primary Purpose:

Prevention

Official Title:

PREvention of STroke in Intracerebral haemorrhaGE Survivors With Atrial Fibrillation (PRESTIGE-AF)

Actual Study Start Date :

Jun 3, 2019

Anticipated Primary Completion Date :

May 31, 2022

Anticipated Study Completion Date :

Nov 30, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Direct Oral Anticoagulant If the patient is randomized in this arm, a direct oral anticoagulant (DOAC) included: Direct thrombin inhibitor: Dabigatran Factor Xa inhibitors: Apixaban or Rivaroxaban or Edoxaban will be prescribed to the patient. Choice and dose of DOAC treatment as well as the use of concomitant medication during the study treatment will be at the Principal Investigator´s discretion within the spectrum of licensed doses labelled for stroke prevention in atrial fibrillation patients in Europe following the Summary of Product Characteristics.	Drug: Apixaban Oral Tablet Factor Xa Inhibitor Other Names: Eliquis Drug: Dabigatran Direct Thrombin Inhibitor Other Names: Pradaxa Drug: Edoxaban Tablets Factor Xa Inhibitor Other Names: Lixiana Savaysa Drug: Rivaroxaban Factor Xa Inhibitor Other Names: Xarelto
No Intervention: No Anticoagulant If the patient is randomized in this arm investigators will use their best judgment to decide upon the prescription of an antiplatelet drug of their choice or no such therapy

Arm

Intervention/Treatment

Experimental: Direct Oral Anticoagulant

If the patient is randomized in this arm, a direct oral anticoagulant (DOAC) included: Direct thrombin inhibitor: Dabigatran Factor Xa inhibitors: Apixaban or Rivaroxaban or Edoxaban will be prescribed to the patient. Choice and dose of DOAC treatment as well as the use of concomitant medication during the study treatment will be at the Principal Investigator´s discretion within the spectrum of licensed doses labelled for stroke prevention in atrial fibrillation patients in Europe following the Summary of Product Characteristics.

Drug: Apixaban Oral Tablet

Factor Xa Inhibitor

Other Names:

Eliquis

Drug: Dabigatran

Direct Thrombin Inhibitor

Other Names:

Pradaxa

Drug: Edoxaban Tablets

Factor Xa Inhibitor

Other Names:

Lixiana

Savaysa

Drug: Rivaroxaban

Factor Xa Inhibitor

Other Names:

Xarelto

No Intervention: No Anticoagulant

If the patient is randomized in this arm investigators will use their best judgment to decide upon the prescription of an antiplatelet drug of their choice or no such therapy

Outcome Measures

Primary Outcome Measures

Time to the first incident ischemic stroke event. [3 years]
Statistics: product-limit estimations of the time to event ("survival") functions in both study groups. Measure of association: hazard ratio under the proportional hazard assumption.
Time to the first recurrent intracerebral haemorrhage event. [3 years]
Statistics: product-limit estimations of the time to event ("survival") functions in both study groups. Measure of association: hazard ratio under the proportional hazard assumption.

Secondary Outcome Measures

Rate of all stroke events [3 years]
Rate of all stroke events from the index date as number of events per 100 person years under observation in the study
Rate of systemic embolism [3 years]
Rate of systemic embolism from the index date as number of events per 100 person years under observation in the study
Rate of major adverse cardiac events [3 years]
Rate of major adverse cardiac events from the index date as number of events per 100 person years under observation in the study
Rate of all-cause mortality [3 years]
Rate of all-cause mortality from the index date as number of events per 100 person years under observation in the study
Rate of cardiovascular mortality [3 years]
Rate of cardiovascular mortality from the index date as number of events per 100 person years under observation in the study
Rate of major haemorrhage [3 years]
Rate of major haemorrhage from the index date as number of events per 100 person years under observation in the study
Rate of any intracranial haemorrhage [3 years]
Rate of any intracranial haemorrhage from the index date as number of events per 100 person years under observation in the study
Rates of events (all strokes, systemic embolic event, myocardial infarction, cardiovascular mortality and major bleeding) [3 years]
Rates of events (all strokes, systemic embolic event, myocardial infarction, cardiovascular mortality and major bleeding) from the index date as number of events per 100 person years under observation in the study
Rate of myocardial infarction [3 years]
Rate of myocardial infarction from the index date as number of events per 100 person years under observation in the study
Rate of major bleedings [3 years]
Rate of major bleedings from the index date as number of events per 100 person years under observation in the study
Quality of life: EQ-5D [enrolment visit, 12 months, 24 months, 36 months]
Quality of life: EQ-5D with 3 levels of severity for each of the 5 dimensions: EQ-5D-3L Statistics at 12, 24 (if required) and 36 months (if required) in both study groups: Measures of central tendency and dispersion (mean and SD resp. median and interquartile range) for EQ VAS score (range 0 -100, higher values considered to be a better outcome) and for the EQ-5D-3L index score (range 0 - 1, higher values considered to be a better outcome) health profile: numbers and proportions reporting frequencies of the three levels within the EQ-5D dimensions in both study groups
Cognitive function: the Montreal Cognitive Assessment (MoCA) [enrolment visit, 12 months, 24 months, 36 months]
Cognitive function: the Montreal Cognitive Assessment (MoCA) Total MoCA score: Range: 0 - 30, higher values considered to be a better outcome. Statistics at 12, 24 (if required) and 36 months (if required) in both study groups: Measures of central tendency and dispersion (mean and SD resp. median and inter quartile range). Frequencies for the values of the subscores in both study groups
Psychological morbidity: the Hospital Anxiety and Depression Scale (HADS) [enrolment visit, 12 months, 24 months, 36 months]
Psychological morbidity: the Hospital Anxiety and Depression Scale (HADS) Statistics at 12, 24 (if required) and 36 months (if required) in both study groups. HADS anxiety and HADS depression score. For both scales range 0 - 21, smaller values considered to be a better outcome. Median score and interquartile range for both scales in both study groups. Numbers and percentages of those patients classified as "non-cases", having mild disease, having moderate disease and having severe disease for both scales in both study groups according to the cut-off scores for HADS quantification.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Age ≥ 18 years
Written informed consent
Recent history of a non-traumatic spontaneous intracerebral haemorrhage during the 6 months before enrolment
Documented evidence of Atrial Fibrillation (paroxysmal, persistent or permanent)
CHA2DS2-VASc score≥2 for male, and CHA2DS2-VASc score≥ 3 for female patients
Availability of brain imaging following the index intracerebral haemorrhage

Exclusion Criteria:

Patient lacks capacity to consent
Fully dependent (Modified Rankin Scale Score >4)
Women who are pregnant, breastfeeding, or plan to become pregnant during the Study period
Women of childbearing potential who are unable or unwilling to take measures for effective contraception
Intracerebral haemorrhage occurring within the last 14 days before enrolment
Intracerebral haemorrhage occurring longer than 6 months before enrolment
Intracerebral haemorrhage resulting from trauma or vascular malformation
Another indication for long-term anticoagulation
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 summary of product characteristics (SmPC).
Absolute need for antiplatelet therapy at enrolment
Presence of a left atrial appendage occlusion device (LAAO) or plan to implant an LAAO
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
Participation in any clinical study with an Investigational Medicinal Product within the past 30 days (observational studies are permitted)

Contacts and Locations

Locations

	Site	City	Country	Postal Code
1	Klinikum Altenburger Land	Altenburg	Germany
2	Vivantes Hospital Neukolin	Berlin	Germany
3	University Hospital Cologne	Cologne	Germany
4	University Hospital Erlangen	Erlangen	Germany
5	Alfried Krupp Von Bohlen und Halbach-Krankenhaus	Essen	Germany
6	University Hospital Frankfurt	Frankfurt	Germany
7	Bezirkskrankenhaus Günzburg	Günzburg	Germany
8	Medizinische Hochschule Hannover	Hannover	Germany
9	University Hospital Heidelberg	Heidelberg	Germany
10	University Hospital Schleswig-Holstein Campus Kiel	Kiel	Germany
11	University of Leipzig	Leipzig	Germany
12	University Hospital Schleswig-Holstein Campus Luebeck	Luebeck	Germany
13	Johannes Wesling Klinikum Minden	Minden	Germany
14	Hospital Germans Trias I Pujol	Barcelona	Spain
15	Hospital Dr Josep Trueta	Girona	Spain
16	East Kent Hospitals University NHS Foundation Trust	Ashford	United Kingdom	TN24 0LZ
17	Northumbria Healthcare NHS Foundation Trust	Ashington	United Kingdom	NE63 9JJ
18	Basildon and Thurrock University Hospitals NHS Trust	Basildon	United Kingdom	SS16 5NL
19	Cambridge University Hospitals NHS Trust	Cambridge	United Kingdom
20	Hull and East Yorkshire NHS Trust	Hull	United Kingdom	HU3 2JZ
21	Kings College Hospital NHS Foundation Trust	London	United Kingdom	SE5 8AF
22	Imperial College Healthcare NHS Trust	London	United Kingdom	W6 8RF
23	Royal Free London NHS Foundation Trust	London	United Kingdom
24	University Hospitals Plymouth NHS Trust	Plymouth	United Kingdom	PL6 8DH
25	St Helens and Knowsley Teaching Hospital NHS Trust	Prescot	United Kingdom	L35 5DR
26	Taunton and Somerset NHS Foundation Trust	Taunton	United Kingdom	TA1 5DA
27	Mid Yorkshire Hospitals NHS Trust	Wakefield	United Kingdom	WF1 4DG
28	West Hertfordshire Hospitals NHS Trust	Watford	United Kingdom	WD18 0HB