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Grant: Project Grant

University of Alberta

$722,926.00

Nimodipine Systemic Exposure and Outcomes Following Aneurysmal Subarachnoid Hemorrhage: A Prospective Multicenter Observational Study (ASH-II Study)

EF 2023-24

Résumé
Aneurysmal subarachnoid hemorrhage (SAH) is a life-threatening neurological illness: it is bleeding in the brain after a bulging blood vessel (a brain aneurysm) ruptures. Although SAH accounts for 5% of all strokes, it often happens in middle age and it puts a significant burden on many patients during their most productive years. Complications following SAH are common, and they can cause major long-term disability. Only one medication - nimodipine - has been proven to benefit the health and wellbeing of these patients. All SAH patients should receive nimodipine for 21 days at a fixed dose. However, our early work suggested that all patients are not getting equal amounts of nimodipine into their blood. In addition, the two different forms (structural mirror images) of nimodipine might have different effects. Reduced amounts of nimodipine in the blood may lessen its benefit and contribute to worsening health and wellbeing of SAH patients. We need to address this knowledge gap immediately. Some patients are likely not getting the full benefit of nimodipine, and most of their doctors are completely unaware of the problem. The overall goal of this research is to see what happens with different nimodipine doses and to confirm whether the two forms of nimodipine have different effects. We will conduct a multi-centre study in adult patients admitted for SAH in Canada and the USA. We will collect blood samples to determine the amount of each type of nimodipine in each participant's body, and we will check to see how each participant is doing at 90 days following SAH. We will also check other factors affecting nimodipine levels, so that we can in the future suggest dose recommendations that are actually tailored to each patient. The findings of this research will help us to understand the potential uses of the different forms of nimodipine and help us to develop personalized nimodipine dosages in SAH patients.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
500010
Name
Mahmoud Sherif H
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Clinical
Prcname2
Behavioural Sciences - B: Clinical Behavioural Sciences
Projecttitle
Nimodipine Systemic Exposure and Outcomes Following Aneurysmal Subarachnoid Hemorrhage: A Prospective Multicenter Observational Study (ASH-II Study)
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$722,926
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Chiral Compound; Nimodipine; Pharmacokinetics; Subarachnoid Hemorrhage
Abstract
Aneurysmal subarachnoid hemorrhage (SAH) is a life-threatening neurological illness: it is bleeding in the brain after a bulging blood vessel (a brain aneurysm) ruptures. Although SAH accounts for 5% of all strokes, it often happens in middle age and it puts a significant burden on many patients during their most productive years. Complications following SAH are common, and they can cause major long-term disability. Only one medication - nimodipine - has been proven to benefit the health and wellbeing of these patients. All SAH patients should receive nimodipine for 21 days at a fixed dose. However, our early work suggested that all patients are not getting equal amounts of nimodipine into their blood. In addition, the two different forms (structural mirror images) of nimodipine might have different effects. Reduced amounts of nimodipine in the blood may lessen its benefit and contribute to worsening health and wellbeing of SAH patients. We need to address this knowledge gap immediately. Some patients are likely not getting the full benefit of nimodipine, and most of their doctors are completely unaware of the problem. The overall goal of this research is to see what happens with different nimodipine doses and to confirm whether the two forms of nimodipine have different effects. We will conduct a multi-centre study in adult patients admitted for SAH in Canada and the USA. We will collect blood samples to determine the amount of each type of nimodipine in each participant's body, and we will check to see how each participant is doing at 90 days following SAH. We will also check other factors affecting nimodipine levels, so that we can in the future suggest dose recommendations that are actually tailored to each patient. The findings of this research will help us to understand the potential uses of the different forms of nimodipine and help us to develop personalized nimodipine dosages in SAH patients.
Competitiondate
202403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Mahmoud, Sherif H
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $722,926~ $0~