Table 8.
Study name | Target population | Intervention | Cognitive function as outcome |
---|---|---|---|
Impact of Anticoagulation Therapy on the Cognitive Decline and Dementia in Patients With Non-Valvular Atrial Fibrillation (CAF), NCT03061006 | Non-valvular AF | Randomization to dabigatran or warfarin | Primary outcome: incident dementia and moderate decline in cognitive function |
Comparison of Brain Perfusion in Rhythm Control and Rate Control of Persistent Atrial Fibrillation, NCT02633774 | Persistent AF | Randomization to rhythm or rate control | Primary outcome: cognitive assessment |
Cognitive Impairment Related to Atrial Fibrillation Prevention Trial (GIRAF), NCT01994265 | AF patients >65 years old and CHA2DS2-VASc >1 | Randomization to dabigatran or warfarin | Primary outcome: cognitive impairment |
Early Treatment of Atrial Fibrillation for Stroke Prevention Trial (EAST), NCT01288352 | AF patients | Randomization to early standardized rhythm control or usual care | Secondary outcome: cognitive function |
Apixaban During Atrial Fibrillation Catheter Ablation: Comparison to Vitamin K Antagonist Therapy (AXAFA), NCT02227550 | Patients undergoing catheter ablation of non-valvular AF | Randomization to vitamin K antagonists or apixaban | Secondary outcome: cognitive function change |
NOACs for Stroke Prevention in Patients With Atrial Fibrillation and Previous ICH (NASPAF-ICH), NCT02998905 | Patients with a high-risk of AF and previous intracerebral haemorrhage | Randomization to non-vitamin K antagonist oral anticoagulant or acetylsalicylic acid | Secondary outcome: cognitive function |
Non-vitamin K Antagonist Oral Anticoagulants in Patients With Atrial High Rate Episodes (NOAH), NCT02618577 | patients with atrial high rate episodes and at least two stroke risk factors but without AF | Randomization to edoxaban or acetylsalicylic acid or placebo | Secondary outcome: cognitive function |
Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atrial Fibrillation Trial (OCEAN), NCT02168829 | Patients having undergone a successful AF catheter ablation | Randomization to rivaroxaban or acetylsalicylic acid | Secondary outcome: neuropsychological testing |
Blinded Randomized Trial of Anticoagulation to Prevent Ischaemic Stroke and Neurocognitive Impairment in AF (BRAIN-AF), NCT02387229 | Patients with non-valvular AF and with low risk of stroke | Randomization to rivaroxaban or acetylsalicylic acid | Primary outcome: composite endpoint of stroke, TIA and neurocognitive decline |
Secondary outcomes: neurocognitive decline, new onset of cognitive impairment |
AF, atrial fibrillation; NOACs, non-vitamin K antagonist oral anticoagulant; TIA, transient ischaemic attack.