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Thalamic and Thalamic Projection Abnormalities on DTI and NODDI Analysis Following Acute Concussion

James Houston,Frank Skidmore,William Monroe, Jon Amburgy,Mitchell Self

Neurology(2019)

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摘要
ObjectiveEvaluate the efficacy and safety of non-invasive vagus nerve stimulation (nVNS) for the treatment of post-traumatic headache (PTH). BackgroundWorldwide, ;69 million people per year sustain a traumatic brain injury (TBI), many of whom develop PTH.Clinicians often treat PTH with drugs approved for primary headache disorders, and many patients selftreat with over-the-counter agents but have inadequate pain relief.There has been little study of therapies for PTH, and safe, effective treatments are needed. Design/MethodsThis randomized, double-blind, sham-controlled, parallel-group pilot study is enrolling adults who present 1-4 weeks after a head injury, meet International Classification of Headache Disorders 3 rd edition (ICHD-3) criteria for acute headache attributed to mild TBI, and have ≥2 headaches/ week with a migraine or probable migraine phenotype.After a 2-week runin period, subjects are randomly assigned (1:1 allocation) to receive daily preventive therapy and as-needed acute treatment with nVNS or a sham device.Preventive therapy consists of two 120-second stimulations 3 times daily.Acute treatment comprises 2 stimulations at headache onset and 2 stimulations 20 minutes after the start of initial treatment.Subjects are not to use acute rescue medication for 120 minutes post-treatment.One North American site will enroll ≤80 subjects.The expected duration is 12 months (enrollment, 9 months; participation, 14 weeks). ResultsThe primary effectiveness end point is decrease in pain (on a 7-point scale) 60 minutes post-treatment for all treated headache attacks.Secondary end points include decrease in the frequency of headache days between the run-in period and the last 2 weeks of the double-blind period and responder rates (ie, percentages of subjects with ≥50% decrease in attack frequency).The primary safety end point is the incidence of treatment-related serious adverse events. ConclusionsThis study will assess the efficacy and safety of nVNS as a novel therapy for PTH.
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