Vasospasm
Conditions
Keywords
Milrinone
Brief summary
Subarachnoid hemorrhage (SAH) is a frequent and severe disease. Mortality can reach 40%. The most frequent complication of SAH is arterial vasospasm, with estimated incidence as high as 70%. Vasospasm is responsible for cerebral ischemia leading to severe morbidity, poorer quality of life and increased mortality. Intravenous Milrinone, because of vasodilatory properties could be a therapeutic option. We hypothesize that intravenous infusion of Milrinone will improve the neurological recovery of patients with vasospasm following aneurysmal SAH at 3 months. This is a Phase III, multi-center, randomized, double-blinded, placebo-controlled study. The primary outcome will be the proportion of patients with a good outcome 3 months (defined as a modified rankin score ≤2).
Detailed description
Subarachnoid hemorrhage (SAH) is relatively frequent, accounting for 5% of strokes, and affects a relatively young population. It is essentially caused by cerebral aneurysm rupture. Mortality can reach 40%. The most frequent complication of SAH is arterial vasospasm, with estimated incidence as high as 70%. Vasospasm is responsible for cerebral ischemia, delayed or not, which in turn is responsible for severe morbidity (neurological deficit, neuro psychiatric disorders...), poorer quality of life (institutionalization, inability to return to work ...) and increased mortality. The pathophysiology of vasospasm is complex, multifactorial and far from being fully understood. Many drugs have been studied in the treatment of symptomatic vasospasm but none has really proven its efficacy. Milrinone is proposed for the treatment of cerebral vasospasm, either as intra-arterial injection (during angiography) or intravenously using continuous infusion. Indeed, among new vasospasm's treatments, Milrinone seems to have good angiographic and clinical results. There is no randomized controlled trials evaluating Milrinone for preventive and/or curative treatment of cerebral vasospasm following aneurysmal SAH. The literature is made only of clinical cases, cases series with angiographic studies or interventional studies not controlled and with no more than 10 patients. Thus we hypothesize that the intravenous infusion of Milrinone will improve the neurological recovery of patients with vasospasm following aneurysmal SAH at 3 months. Adult patients, hospitalized for a vasospasm complicating subarachnoid hemorrhage secondary to intracranial aneurysm rupture will be included and randomized within 6 hours of the CT-scanner confirming the vasospasm diagnosis to receive either the study drug (milrinione, a 0,1 mg/kg bolus followed by a 1 μg/kg/min perfusion) or placebo (saline, with a bolus and a continuous infusion). Study drug administration will be formalized (minimum duration 48 hours, maximum duration 14 days).The primary endpoint will be the proportion of patients with a good outcome 3 months (defined as a modified rankin score ≤2).
Interventions
Blinding procedure will be set up for the administration of the treatment
Blinding procedure will be set up for the administration of the treatment
Sponsors
Study design
Intervention model description
Phase 3, multicenter, international (France, Switzerland), randomized, double blinded, placebo-controlled study
Eligibility
Inclusion criteria
* Adult patients hospitalized for aneurysmal SAH * First episode of vasospasm, with a diagnosis confirmed on cerebral arterial CT-scanner * Delay between diagnosis of vasospasm (done by CT-scanner) and inclusion ≤6 hours * Informed consent from a legal representative, or emergency procedure
Exclusion criteria
* Initial Glasgow score at 3 with a bilateral mydriasis * Moribund patient * Contraindication to Milrinone (notably obstructive cardiomyopathy…) * Cerebral infarction in the vasospasm area already present on the CT-scanner at the time of diagnosis (lack of expected benefit of treatment in this case according to medical judgement) * Cardiac failure requiring inotrope administration at the time of randomisation * Uncontrolled elevated intra-cranial pressure (i.e. ICP\>25 mmHg for more than 20 minutes) * Patient with flutter or cardiac arrhythmia (atrial fibrillation) poorly tolerated * Major metabolic disturbance (uncorrected hypokalaemia \<3 mmol/L) * Non-affiliation to French health care coverage, * Pregnant, breastfeeding or parturient woman * Adult deprived of their liberty by judicial or administrative decision * Adult under compulsory psychiatric care * Adult patient protected under the law (guardianship or trusteeship) * Inclusion in an interventional study using Milrinone, or evaluating a treatment of cerebral vasospasm or with the same primary endpoint (mRS at 3 months).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of patients with a good outcome at 3 months | 3 months | modified Rankin score ≤2 (0 = No symptoms, 1 = No significant disability. Able to carry out all usual activities, despite some symptoms, 2 = Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities, 3 = Moderate disability. Requires some help, but able to walk unassisted, 4 = Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted, 5 = Severe disability. Requires constant nursing care and attention, bedridden, incontinent, 6 = Death) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mortality rates in intensive care and in hospital | up to 6 months | To assess mortality rates in intensive care unit and in hospital and 6 months after aneurysm rupture. |
| Modified Rankin Score at 3 and 6 months | 3 and 6 months | 0 = No symptoms, 1 = No significant disability. Able to carry out all usual activities, despite some symptoms, 2 = Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities, 3 = Moderate disability. Requires some help, but able to walk unassisted, 4 = Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted, 5 = Severe disability. Requires constant nursing care and attention, bedridden, incontinent, 6 = Death |
| Glasgow outcome scale Extended at 3 and 6 months | up to 6 months | 1= Death, 2=Persistent vegetative state, 3=Sever disability, 4=Moderate disability, 5=Good recovery 2. Persistent vegetative state 3\. Severe disability 4. Moderate disability 5. Low disability |
| EQ-5D | up to 6 months | Obtained by centralized telephone interview |
| Evaluation of the radiologic effectiveness of the treatment | up to 14 days | Evaluation of the angiographic success according to angiographic CT-scannerwith blind analysis (coted as follows: light success, moderate success or important success) |
| Evaluation of the hemodynamic tolerance of the treatment | 24 hours | need to introduce and/or increase doses of catecholamines by + 50% during the first 24 hours |
| Evaluation of the metabolic tolerance of the treatment | up to 14 days | The occurrence of dysnatremia (\<135 mmol / L or\> 155 mmol / L), Daily diuresis. |
| cerebral artery flow velocities | H0, H+2, H24+/-12h, H48+/-12h | Describe treatment-related variations in middle cerebral artery flow velocities. |
| Length of stay in the intensive care unit and in the hospital | 3 months | Number of days alive in the intensive care unit and in the hospital |
| live patient rate | 3 months and 6 months | — |
| Describe the number of therapeutic arteriographies | Day 14 | number of artheriographies |
Countries
France
Contacts
University Hospital of Nantes
Cavale Blanche - University Hospital of Brest
Hôpital Gui de Chauliac - University Hospital of Montpellier
Hôpital de Hautepierre, University Hospital of Strasbourg
Hôpital Gabriel Montpied, University Hospital of Clermont-Ferrand
Hôpital Lariboisière, Paris (AP-HP)
Hôpital Bretonneau - University Hospital of Tours
University Hospital of Rennes
University Hospital of Poitiers
University Hospital of Dijon