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Active, not recruiting Observational

Impact of Platelet Activation in Intracranial Aneurysm Rupture Risk - PLAQRAN

NCT03408379 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2017-12-20
Last updated
2026-01-20

Condition(s) studied

Intracranial AneurysmsRuptured Aneurysm

Investigational drug(s) / intervention(s)

Collection of blood sample in aneurysm

Collection of blood sample in aneurysm: In case of an endovascular treatment : * A blood sample (venous or arterial) of 10 ml will be taken at the beginning of the procedure, an intra aneurysmal blood sample (1mL) will be taken during the procedure and a blood sample (arterial) of 1 mL will be taken at the end of the procedure. * Iterative blood samples (arterial) of 10 mL will be taken at each follow up visit. In case of a surgery treatment : * A blood sample (venous or arterial) of 10 ml will be taken at the beginning of the surgery. * A Tissue sample will be taken during the surgery * Iterative blood samples (arterial) of 10 mL will be taken at each follow up visit.

Study summary

Sub arachnoid hemorrhage consecutive to intracranial aneurysm rupture is a devastating disease. Predictors of intracranial aneurysm rupture are limited and focus mainly on size and location. Platelet activation may have a deleterious role on aneurysm rupture. The assumption is that patients with ruptured intracranial aneurysm will present a higher rate of platelet activation compared to patients with non ruptured aneurysms.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient aged 18 and over * Patient presenting a single or multiple aneurysm * Patient presenting an intracranial aneurysm for which an intervention is planned (endovascular treatment or surgery) : elective intervention for an unruptured aneurysm or emergency surgery for a broken aneurysm Exclusion Criteria: * Pregnant or breast feeding woman * Patient benefiting from legal protection measures

Primary outcome measure(s)

  • Proportion of patients with platelet activation — in the 7 days before embolisation
    comparison of this proportion between patients with ruptured versus non ruptured intracranial aneurysm

Trial sites (1)

FacilityCityRegionStatus
Fondation Ophtalmologique A. de Rothschild Paris France
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 NCT03408379 on ClinicalTrials.gov ↗ ← All trials in France