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Milrinone Infusion for VAsospam Treatment in Subarachnoid hemoRrhage

Milrinone Infusion for VAsospam Treatment in Subarachnoid hemoRrhage

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04362527
Acronym
MIVAR
Enrollment
370
Registered
2020-04-27
Start date
2020-08-10
Completion date
2026-01-12
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vasospasm

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

DRUGMilrinone 1 Mg/mL Solution for Injection

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

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Intervention model description

Phase 3, multicenter, international (France, Switzerland), randomized, double blinded, placebo-controlled study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Proportion of patients with a good outcome at 3 months3 monthsmodified 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

MeasureTime frameDescription
Mortality rates in intensive care and in hospitalup to 6 monthsTo assess mortality rates in intensive care unit and in hospital and 6 months after aneurysm rupture.
Modified Rankin Score at 3 and 6 months3 and 6 months0 = 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 monthsup to 6 months1= 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-5Dup to 6 monthsObtained by centralized telephone interview
Evaluation of the radiologic effectiveness of the treatmentup to 14 daysEvaluation 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 treatment24 hoursneed to introduce and/or increase doses of catecholamines by + 50% during the first 24 hours
Evaluation of the metabolic tolerance of the treatmentup to 14 daysThe occurrence of dysnatremia (\<135 mmol / L or\> 155 mmol / L), Daily diuresis.
cerebral artery flow velocitiesH0, H+2, H24+/-12h, H48+/-12hDescribe treatment-related variations in middle cerebral artery flow velocities.
Length of stay in the intensive care unit and in the hospital3 monthsNumber of days alive in the intensive care unit and in the hospital
live patient rate3 months and 6 months
Describe the number of therapeutic arteriographiesDay 14number of artheriographies

Countries

France

Contacts

PRINCIPAL_INVESTIGATORKarim KL LAKHAL, PH

University Hospital of Nantes

PRINCIPAL_INVESTIGATOROlivier OH HUET, PU-PH

Cavale Blanche - University Hospital of Brest

PRINCIPAL_INVESTIGATORPierre-François PP PERRIGAULT, PU-PH

Hôpital Gui de Chauliac - University Hospital of Montpellier

PRINCIPAL_INVESTIGATORJulien JP POTTECHER, PU-PH

Hôpital de Hautepierre, University Hospital of Strasbourg

PRINCIPAL_INVESTIGATORRussel RC CHABANNE, PH

Hôpital Gabriel Montpied, University Hospital of Clermont-Ferrand

PRINCIPAL_INVESTIGATORBenjamin BC Chousterman, PH

Hôpital Lariboisière, Paris (AP-HP)

PRINCIPAL_INVESTIGATORMarc ML Laffon, PU-PH

Hôpital Bretonneau - University Hospital of Tours

PRINCIPAL_INVESTIGATORYoann YL Launey, PH

University Hospital of Rennes

PRINCIPAL_INVESTIGATORClaire CD Dahyot Fizelier, PU-PH

University Hospital of Poitiers

PRINCIPAL_INVESTIGATORBelaid BB Bouhemad, PU-PH

University Hospital of Dijon

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026