Skip to content

Interest of Molecular Analysis of Cerebral Thrombi in Determining the Prognosis and Etiology of Cerebral Infarction

Interest of Molecular Analysis of Cerebral Thrombi in Determining the Prognosis and Etiology of Cerebral Infarction

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05658835
Acronym
MATISSE
Enrollment
311
Registered
2022-12-21
Start date
2023-02-08
Completion date
2025-02-28
Last updated
2024-01-31

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

Conditions

Ischemic Stroke

Keywords

ischemic stroke, thrombi, metabolites

Brief summary

The MATISSE (Molecular Analysis of Thrombus for Ischemic Stroke prognosis and Etiology) project evaluates the hypothesis that the molecular composition of cerebral thrombus in metabolites, lipids, and proteins conditions the clinical prognosis at 3 months of the infarction and informs on its etiological subtype

Interventions

OTHERThrombi and blood analyses

Thrombi and blood will be collected during thrombectomy

Sponsors

Assistance Publique Hopitaux De Marseille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Male or female 18 years of age or older; * Patient with a cerebral infarction documented by brain imaging who received endovascular treatment by mechanical thrombectomy; * Patient for whom it was possible to collect cerebral thrombus for LC-MS analysis during mechanical thrombectomy: * Patient who was informed of the study and formulated a non-opposition to participation. If not, patient for whom a relative was informed and formulated a non-opposition.

Exclusion criteria

* Patient with a cerebral infarction documented by cerebral imaging, having benefited from an endovascular treatment with mechanical thrombectomy that did not allow the extraction of a cerebral thrombus. * Protected persons (articles L1121-5, L1121-6 and L121-8 of the Public Health Code): pregnant or breast-feeding women, persons deprived of liberty, under guardianship or curatorship

Design outcomes

Primary

MeasureTime frameDescription
Determination and validation of molecular signatures, obtained by LC-MS analysis of cerebral thrombi, predictive of the excellent clinical prognosis3 months after the cerebral infarctionRankin score (0 to 6, 6 meaning worse outcome)

Secondary

MeasureTime frameDescription
Death3 months after cerebral infarctionDeath of the patient
Determination of molecular signatures predictive on successful recanalization after mechanical thrombectomyRight after the thrombectomyScore mTICI (modified Thrombolysis In Cerebral Infarction, 0 to 3, 0 meaning worst outcome)
Determination and validation of molecular signatures, obtained by LC-MS analysis7 days after the cerebral infarctionASCOD (atherosclerosis, small vessel disease (SVD), cardioembolism, other and dissection) description (0 to 9, 9 meaning insufficient assessment to determine the presence or absence of the disease)
Severe intracranial hemorrhage3 months after the cerebral infarctionHeildeberg classification (0 to 3d, 3d meaning subdural hemorrhage)
Positive infarct growth after successful recanalizationBetween 24 and 48h after the thrombectomyQuantification of infarctus volume by MRI
Early Neurological Deterioration24 hours after recanalization treatmentWorsening of at least 4 points in the NIHSS (National Institutes of Health Stroke Scale) score (0 meaning better outcome, 0 to 42)
Use of thrombolytic therapy in the acute phaseBefore thrombectomyQuantification of thrombolytic therapy
Patient exposure to peak outdoor air pollution96 hours before cerebral infarctionQuantification of peak outdoor air pollution (identification of the location of the patient and the polluants observed in the areas)
Recovery of autonomy in walking3 months after the cerebral infarctionParker score (0 to 9, 9 meaning better outcome)

Countries

France

Contacts

Primary ContactEmilie Doche
emilie.doche@ap-hm.fr04 91 38 78 65

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026