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Thrombus Composition in Ischemic Stroke: Analysis of the Correlation With Plasma Biomarkers, Efficacy of Treatment, Etiology and Prognosis (COMPO-CLOT)

F

Fondation Ophtalmologique Adolphe de Rothschild

Status

Enrolling

Conditions

Etiology
Biomarkers
Biological Specimen Banks
Stroke, Acute
Prognosis

Treatments

Other: Collection of thrombus that is responsible for stroke and blood sample

Study type

Observational

Funder types

NETWORK

Identifiers

NCT03268668
JDS_2017_8

Details and patient eligibility

About

The recent validation of thrombectomy in addition to thrombolysis with intravenous administration of alteplase suggests a major revolution in the management of acute strokes. This treatment option also opens up a new field of research, making possible the analysis of the clot responsible for intracranial occlusion. Indeed, in about 30% of the cases, the thrombectomy procedure makes it possible to retrieve either partially or completely the clot. Previous studies have analyzed the correlation between the composition of the thrombus and the etiology of stroke. Their discordant results do not yet make it possible to distinguish a particular profile of thrombus according to etiology. Other studies have shown a correlation between the proportion of red blood cells in a thrombus and the likelihood that it is visible in MRI or cerebral scanning. More recently, one study has demonstrated a correlation between the presence of lymphocytes in the thrombus and an atheromatous etiology.

The main limitations of these studies are the small number of patients included, the high variability of conservation protocols and the absence of plasma data, which does not allow for research on the correlation between clot composition and plasma biomarkers.

Enrollment

1,200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18 years and older
  • Presenting with cerebral infarction following arterial occlusion
  • Treated for mechanical thrombectomy (whether performed or not)
  • Free, informed, and express consent of the patient or their relatives (emergency inclusion procedure)
  • For retrospective patients: thrombus already collected (according to the center's usual practice or for another research project).

Exclusion criteria

  • Patient benefiting from a legal protection measure
  • Pregnant or breastfeeding woman

Trial contacts and locations

12

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Central trial contact

Jean-Philippe Désilles, MD; Amélie Yavchitz, MD PhD

Data sourced from clinicaltrials.gov

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