학술논문

Selecting Patients for Intra-Arterial Therapy in the Context of a Clinical Trial for Neuroprotection
Document Type
article
Source
Stroke. 47(12)
Subject
Clinical Research
Stroke
Clinical Trials and Supportive Activities
Brain Ischemia
Clinical Protocols
Clinical Trials as Topic
Double-Blind Method
Humans
Mechanical Thrombolysis
Neuroprotective Agents
Patient Selection
Protein C
Recombinant Proteins
Thrombolytic Therapy
activated protein C
clinical trial
neuroprotective agents
thrombectomy
thrombolysis
Cardiorespiratory Medicine and Haematology
Clinical Sciences
Neurosciences
Neurology & Neurosurgery
Language
Abstract
Background and purposeThe advent of intra-arterial neurothrombectomy (IAT) for acute ischemic stroke opens a potentially transformative opportunity to improve neuroprotection studies. Combining a putative neuroprotectant with recanalization could produce more powerful trials but could introduce heterogeneity and adverse event possibilities. We sought to demonstrate feasibility of IAT in neuroprotectant trials by defining IAT selection criteria for an ongoing neuroprotectant clinical trial.MethodsThe study drug, 3K3A-APC, is a pleiotropic cytoprotectant and may reduce thrombolysis-associated hemorrhage. The NeuroNEXT trial NN104 (RHAPSODY) is designed to establish a maximally tolerated dose of 3K3A-APC. Each trial site provided their IAT selection criteria. An expert panel reviewed site criteria and published evidence. Finally, the trial leadership designed IAT selection criteria.ResultsDerived selection criteria reflected consistency among the sites and comparability to published IAT trials. A protocol amendment allowing IAT (and relaxed age, National Institutes of Health Stroke Scale, and time limits) in the RHAPSODY trial was implemented on June 15, 2015. Recruitment before and after the amendment improved from 8 enrolled patients (601 screened, 1.3%) to 51 patients (821 screened, 6.2%; odds ratio [95% confidence limit] of 4.9 [2.3-10.4]; P