The purpose of this retrospective study is to test the hypothesis that uncontrolled
tachycardia serves as a risk factor for adverse cardiovascular events and poor outcome after
Subarachnoid Hemorrhage (SAH).
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Locations near you
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Full eligibility criteria for NCT01585311
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Age >=18 years
Diagnosis of subarachnoid hemorrhage established by computed tomography (CT scan) or xanthochromia of the cerebrospinal fluid if the CT is negative
Written informed consent from either the patient or a family member
Admitted to the NICU for at least 12 hours
Age < 18yrs
SAH due to a rupture of an arteriovenous malformation, neoplasm vasculitis or other secondary causes
All locations for NCT01585311
United States (1)
New York, New York, United States, 10032
View full eligibility
Tris trial is registered with FDA with number: NCT01585311. The sponsor of the trial is Columbia University and it is looking for 1540 volunteers for the current phase.
Official trial title: Impact of Prolonged Tachycardia on Cardiovascular Morbidity and Outcome After Subarachnoid Hemorrhage (SAH)
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