Paediatric Arteriopathy Steroid Aspirin Project

Arterial Ischemic Stroke Clinical Trial

— PASTA  

Official title:

High Dose Steroids in Children With Stroke and Unilateral Focal Arteriopathy: Paediatric Arteriopathy Steroid Aspirin (PASTA) Project. A Multicentre Randomized Trial.

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT03249844
• Other study ID #: 1608184
• Secondary ID: 2017-002247-15
• Status: Withdrawn
• Phase: Phase 3
• Start date: September 1, 2022
• Est. completion date: December 31, 2027

Study information

• Verified date: October 2022
• Source: Centre Hospitalier Universitaire de Saint Etienne
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Arterial ischemic stroke (AIS) is a devastating condition, affecting 1.6-5/100,000 children/year. Although their outcome is different, children with stroke do not recover better than adults, with at least 2/3 suffering long term sequels such as developmental (motor, global intellectual, language...) and behavioral disabilities, epilepsy, and low adaptative and academic skills... Stenotic cerebral arteriopathy is identified as AIS etiology in 60-80% of previously healthy children and the course of this arteriopathy is the strongest predictor of recurrent events. 30-40% of these children have a focal unilateral cerebral arteriopathy (FCA). Childhood FCA is suspected to be an inflammatory vessel wall pathology triggered by varicella and other (viral) infections. As recurrences occur for the great majority in the first 6 months after the index event, aspirin 5 mg/kg/day is recommended for at least 18 months to 2 years. As there is a rational for using immunomodulatory drugs at the acute stage of FCA, immunotherapies are currently used by neuropaediatricians in AIS, mainly as steroids for children with stenosing arteriopathies. However, due to weak evidences, the literature cannot either encourage or discourage this practice. The long term course of children with FCA is only approach to date by retrospective studies and controversies about outcome remain (for example, the recurrence risk on antithrombotic treatment varies notably from quasi zero to 25%). And finally, it is shown in childhood stroke, as well as in the global field of longstanding impairment, that parental and medical points of view do not match consistently. Longitudinal studies are needed to deserve this familial approach.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 31, 2027
• Est. primary completion date: December 31, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Months to 15 Years

Eligibility

Inclusion Criteria:

-- Aged 6 months to <15 years

• AIS = 48 hours
• Newly acquired focal neurological deficit with confirmation by magnetic resonance imaging (MRI) of ischaemic lesion in an arterial territory corresponding with the clinical features (definition of Arterial ischemic stroke).
• Magnetic resonance arteriography showing unilateral proximal stenosis or irregularities of the corresponding carotid trifurcation (i.e. terminal carotid and/or M1-M2 and/or A1 segments) or of the posterior circulation (P1-P2 segments).
• No evidence of an underlying systemic disorder (e.g. lupus erythematodes) explaining the features.
• Informed and signed consent of parents or legal guardians.
• French Social Security (Sécurité sociale; i.e. national health coverage) affiliation

Exclusion Criteria:

• Children with secondary central nervous system angiitis due to infections (meningitis, endocarditis, borreliosis), rheumatic or other systemic inflammatory diseases (e.g. lupus erythematodes). These children are already under immune suppression or need other co-medications regarding their underlying disease.
• Children with known syndromal and/or genetic vasculopathies such as phaces syndrome, Neurofibromatosis type 1, trisomy 21.
• Children with moyamoya or sickle cell disease.
• Children with a progressive large to medium vessel childhood primary angiitis of the central nervous system with two out of the following three criteria : Children with progressive neurocognitive dysfunction; Children with bilateral lesions/vessel involvement; Children with distal arterial stenosis (beyond the M2, A1 or P2 segment).
• Children already on steroid treatment at disease onset or with a contraindication to receive steroid treatment (e.g. congenital or acquired immunodeficiency).
• Children with delayed diagnosis =3 days as treatment start is not allowed to be more =5 day-delayed.
• Contraindications to steroids (see also summary of product characteristics in chapter 1.1) and notably: Not-manageable infectious, hydro-electrolytic or metabolic (e.g. diabetes mellitus) disorders, or elevated blood pressure, Serious behavioral disorders, Current vaccination with live or attenuated live strains, Allergy/sensibility to any ingredient, Association with some medications such as antiarrhythmic drugs.

Related Conditions & MeSH terms

• Arterial Ischemic Stroke
• Ischemic Stroke
• Stroke

Intervention

Drug:
• Methylprednisolone + prednisolone
The experimental intervention consists of 5 consecutive days Methylprednisolone at a daily single intravenous dose of 20 mg/kg body-weight (max 1 g/day) followed by a 4-week course of tapering Prednisolone given at a daily single oral dose in the morning: week 1 and 2, oral Prednisolone 1 mg/kg/day (max 40 mg/day), , week 3 and 4, oral Prednisolone 0,5 mg/kg/day (max 20 mg/day),

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Saint Etienne	Ministry of Health, France

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to recovery up to 12 months	Evaluate of time to recovery up to 12 months by score paediatric Recurrence and Recovery Questionnaire (RRQ )	Up to 12 months
Secondary	Improvement of functional outcome by face-to-face visits	Evaluate of Improvement of functional outcome by face-to-face visits by score Paediatric Stroke Outcome Measure (PSOM), modified Rankin Scale (mRS) and Vineland Adaptive Behaviour Scale (VABS).	Months:1,6,12, 24 and 36
Secondary	Arteriopathic course along time	Evaluate of Arteriopathic course along time by comparison between magnetic resonance (MR) arteriography and initial imaging.	Months: 1, 6, 24
Secondary	Recurrence of stroke, epilepsy, neurological and developmental sequels, and academic achievement	Evaluate recurrence of stroke, epilepsy, neurological and developmental sequels, and academic achievement at 6, 12, 24 and 36 months. Neurological outcome will be assessed by standard clinical examination: motricity, sensibility, coordination, oculomotricity and visual field, cranial nerves…	Months: 1, 3, 6,12, 24 and 36
Secondary	Outcome by age group	Evaluate outcome by age group. All endpoints will be stratified for the whole cohort by the following age group: 0.5-3 years; 3-6 years; 6-10 years and =10 years. This will be done in a centrally-manner at Clinical Trials Unit (CTU) Bern.	Months 72
Secondary	Familial impact	Evaluate of familial impact by Alberta Perinatal Stroke Parental Outcome Measure (APSOM) and indepth interview through semi-structured interviews. The objective is to report the lived experience of parents whose child was included in the study.	Months 72
Secondary	Number of serious adverse events	Analysis of number of serious adverse events and their cause, consequence.	Months 72