Sub Arachnoid Hemorrhage (SAH) is a public health concern because of its high incidence
(7/100 000 inhab.), its mortality rate (25%), and its morbidity rate (50%).
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Full eligibility criteria for NCT02894034
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Patients 18 years or older
Patient admitted to the Neurosurgical Urgent Care Unit for SAH following a ruptured aneurysm
Patients or one of their loved ones providing written informed consent
Patients with healthcare coverage
Unavailability of a CTc in the initial phase (within the first 12 hours) or absence of 1-mm slices from the scan
Trauma to the optic globe or optic nerve pathology
Preexisting anomalies of ICP or history of neurosurgical cerebral pathologies
SAH of non aneurysm origin (e.g. arterio-venous malformation (AVM), tumor, trauma, sepsis)
Patients under legal protection
All locations for NCT02894034
Amiens, France, 80054
View full eligibility
Tris trial is registered with FDA with number: NCT02894034. The sponsor of the trial is Centre Hospitalier Universitaire, Amiens and it is looking for 114 volunteers for the current phase.
Official trial title: Is the Measured Diameter of the Optic Nerve Sheath by Cerebral Scan in Patients With Early Phase Meningeal Hemorrhage Due to a Ruptured Aneurysm a Prognostic 6-month Mortality Factor?
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