Background: We assessed the occurrence of neurological deficits that may impede the capacity to provide consent for trial participation in patients with an acute stroke, who are eligible for endovascular treatment (EVT). Methods: We used data from the Multicenter Randomized Controlled Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands Registry, a prospective observational cohort study. We included 1526 patients with an anterior large vessel occlusion, undergoing EVT between March 2014 and June 2016. We based our assessment of decision-making capacity for trial participation on neurological symptoms influencing conditions concerning informed consent as stated in the declaration of Helsinki. We formulated a strict an...
Background: Obtaining informed consent for intravenous thrombolysis in acute ischemic stroke can be ...
Background Evidence regarding whether imaging can be used effectively to select patients for endovas...
Background: Endovascular therapy (EVT) for acute ischemic stroke due to proximal occlusion of the an...
Background: We assessed the occurrence of neurological deficits that may impede the capacity to prov...
Background: Obtaining informed consent for a patient's participation in a randomized trial of treatm...
<p><b>Background and Purpose:</b> European directives and legislation in some coun...
Objective: To determine whether the manner of consent, i.e., informed consent by patients themselves...
Background: Clinical trials are the hallmark of evidence-based medicine, but recruitment is often ch...
Successful implementation of a randomized clinical trial (RCT) for neuro-vascular emergencies such a...
BACKGROUND: Endovascular therapy (EVT) for acute ischemic stroke due to proximal occlusion of the an...
International audienceBACKGROUND:The provision of informed consent is a prerequisite for inclusion o...
Goal: Insufficient data is available about safety and efficacy of endovascular treatment (EVT) in pa...
Background: Obtaining informed consent for intravenous thrombolysis in acute ischemic stroke can be ...
Background Evidence regarding whether imaging can be used effectively to select patients for endovas...
Background: Endovascular therapy (EVT) for acute ischemic stroke due to proximal occlusion of the an...
Background: We assessed the occurrence of neurological deficits that may impede the capacity to prov...
Background: Obtaining informed consent for a patient's participation in a randomized trial of treatm...
<p><b>Background and Purpose:</b> European directives and legislation in some coun...
Objective: To determine whether the manner of consent, i.e., informed consent by patients themselves...
Background: Clinical trials are the hallmark of evidence-based medicine, but recruitment is often ch...
Successful implementation of a randomized clinical trial (RCT) for neuro-vascular emergencies such a...
BACKGROUND: Endovascular therapy (EVT) for acute ischemic stroke due to proximal occlusion of the an...
International audienceBACKGROUND:The provision of informed consent is a prerequisite for inclusion o...
Goal: Insufficient data is available about safety and efficacy of endovascular treatment (EVT) in pa...
Background: Obtaining informed consent for intravenous thrombolysis in acute ischemic stroke can be ...
Background Evidence regarding whether imaging can be used effectively to select patients for endovas...
Background: Endovascular therapy (EVT) for acute ischemic stroke due to proximal occlusion of the an...