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CONFIDENTIALASTROH ProtocolAneurysmal Subarachnoid Hemorrhage Trial Randomizing : Continuous Low does Intravenous Therapy in Coiled Low grade Aneurysm Subarachnoid Hemorrhage Patients with Significant
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Gather all necessary documents and information required for filling out the phase I intracranial stenting form.
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Include information about the healthcare provider who will be performing the stenting procedure.
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Who needs phase i intracranial stenting?

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Phase I intracranial stenting is typically needed by individuals who have been diagnosed with intracranial stenosis.
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This condition refers to the narrowing of the blood vessels within the brain, which can lead to reduced blood flow and potential neurological complications.
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Patients who have experienced transient ischemic attacks (mini-strokes) or strokes related to intracranial stenosis may require this procedure to improve blood flow and prevent future complications.
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The decision to undergo phase I intracranial stenting is usually made by a team of healthcare professionals, including neurologists, interventional radiologists, and neurosurgeons, based on the patient's individual case and medical history.
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Phase I intracranial stenting refers to a preliminary stage of a clinical or regulatory process where intracranial stenting procedures are assessed, often focusing on the safety and efficacy of the stent devices used in treating conditions such as aneurysms or arterial stenosis.
Healthcare providers, regulatory bodies, or clinical researchers involved in the implementation or study of intracranial stenting procedures may be required to file documentation related to Phase I intracranial stenting.
To fill out Phase I intracranial stenting forms, individuals typically need to provide relevant patient information, details about the stenting procedure, device specifications, and any associated clinical outcomes, following the guidelines set by the regulatory authority.
The purpose of Phase I intracranial stenting is to evaluate the initial safety, feasibility, and technical aspects of stenting procedures prior to larger clinical trials or general implementation in clinical practice.
Information that must be reported includes patient demographics, procedure details, device used, complications, outcomes, and any follow-up evaluations or data.
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