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Clinical Trials in France / NCT06784518
Starting soon Not applicable

Stroke Cerebral Reorganization Pathways (SPECTRE)

NCT06784518 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-09-01
Last updated
2026-04-02

Condition(s) studied

Brain DiseasesIschemic StrokeStrokeBrain InfarctionStroke Rehabilitation

Investigational drug(s) / intervention(s)

Clinical scores and functional MRI

Clinical scores and functional MRI: Motor evoked potentials between Day 3-Day 7 of the stroke, for a equal distribution of patients into three prognostic groups according to the PREP2 algorithm (good, limited and poor). Longitudinal follow-up with clinical scores and functional MRI at Day 7-Day 10, Day 30, Month 3 and Month 6 of stroke.

Study summary

SPECTRE is a prospective longitudinal study in order to identify whether patients with different degrees of motor recovery are distinguished by distinct brain post-stroke plasticity patterns in the acute and sub-acute phases. This study allows close longitudinal follow-up of patients with severe clinical motor impairment using functional MRI to study cerebral neuroplasticity after ischemic stroke in the acute and sub-acute phase in patients with upper limb motor impairement, taking into account prognostic criteria used in current practice.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Adult (age greater than or equal to 18 years) less than 75 years of age, both sexes; * single supratentorial ischemic stroke confirmed by brain imaging * Upper limb deficit defined by a SAFE score \<5 (SAFE Stinear protocol, prognosis of post-stroke upper limb recovery) on D3 of stroke. This corresponds to the sum of shoulder abduction and finger extension according to the MRC (Medical Research Council) scale for each of these movements out of 5. * Absence of comprehension disorders limiting participation; * Patient covered by french social security; * Free, informed and written consent signed by the patient or a member of the patient's family (in the case of a patient who is able to understand the information and give consent but has motor difficulties resulting in an invalid signature). Non-Inclusion Criteria: * Multiple ischemic strokes or history of clinically significant stroke ; * Posterior fossa stroke ; * Hemorrhagic stroke; * Patient who have undergone thrombolysis or mechanical thrombectomy; * Extensive Fazekas grade 3 vascular leukopathy; * Pre-existing neurodegenerative pathology; * Patient with severe dyspnea or swallowing disorders who cannot undergo brain MRI; * Adults under legal protection (safeguard of justice, curatorship, guardianship, family habilitation), persons deprived of liberty; * Women declaring that they are pregnant or breast-feeding; * Patient participating in another therapeutic or drug intervention study that may have an impact on the effect of cerebral neuroplasticity on the SPECTRE study; * Patients with contraindications to MRI pacemaker or implantable defibrillator, neurosurgical clips, cochlear implants, intra-orbital or encephalic metallic foreign bodies, stents placed less than 4 weeks ago and osteosynthesis devices placed less than 6 weeks ago, claustrophobia. Exclusion Criteria: * If the prognostic group according to the PREP2 algorithm (good, limited and poor) has already been reached during motor evoked potential assessment the patient is excluded. * Recurrence of clinically significant stroke (with worsening NIHSS score \> 4) during study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Rennes Chu Rennes France

More Rennes University Hospital trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06784518 on ClinicalTrials.gov ↗ ← All trials in France