Please sign in to follow a disease.
New risk score could predict strokes in heart patients despite blood thinners
NCT ID NCT07713537
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This study aims to create a better way to predict stroke risk in people with atrial fibrillation (an irregular heartbeat) who are already taking direct oral anticoagulants (DOACs), a type of blood thinner. Even with these medications, some patients still have strokes. Researchers will analyze data from 250 patients to design a risk scale that includes clinical, demographic, and other factors. The goal is to identify who remains at high risk so doctors can tailor treatment more effectively.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could give doctors a better tool to predict stroke risk in atrial fibrillation patients taking blood thinners, potentially preventing strokes.
- What could go wrong
- This is an observational study to develop a risk scale, not a treatment trial. The scale may not prove accurate enough for widespread use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 250 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jan 2025
- Expected to finish
-
Dec 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with a history of AF and on DOAC therapy.
- Ages
-
Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient over 18 years of age * History of AD * Currently on DOACs. * Capacity to understand the study procedures and provide informed consent. Exclusion Criteria: * Patient with valvular AF (mitral stenosis) or mechanical valve prostheses. * Unable to complete a follow-up period of at least 3 months from enrollment.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Atrial fibrillation (AF) are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
2 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Germans Trias University Hospital
RECRUITINGBarcelona, Barcelona, Spain
-
Vall d'Hebron University Hospital
RECRUITINGBarcelona, Barcelona, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Intra-arterial neuroprotective strategy for ischemic STroke patients with no reperfusion therapy (INSIST-NRT): one single center, safety and feasibility study
- Closed-Loop stimulation combined with left bundle branch area pacing in patients with atrioventricular conduction disorders
- Development and evaluation of the effectiveness of a mobile individual atrial fibrillation management (m-BAFY) program
- Drug-eluting stenting versus medical treatment alone for patients with extracranial vertebral artery stenosis: the VISTA trial
- Emergency stroke unit for acute cerebrovascular events: a prospective, single-arm trial with a historical control group
- A prospective, multicenter, randomized controlled, non-inferiority clinical trial evaluating the safety and efficacy of cardiac pulsed field ablation devices combined with single-use spherical pulsed ablation catheters in treating paroxysmal atrial fibrillation