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Biology of Cerebral Arteriovenous Malformations and Prognosis of Cerebral Arteriovenous Malformations

Biology of Cerebral Arteriovenous Malformations : Study of the Link Between Blood Biomarkers and the Haemorrhagic Prognosis of Cerebral Arteriovenous Malformations

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03676868
Acronym
BioMAV
Enrollment
300
Registered
2018-09-19
Start date
2018-11-20
Completion date
2028-11-19
Last updated
2025-06-25

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

Conditions

Cerebral Arteriovenous Malformations, Ruptured or Unruptured Cerebral Arteriovenous Malformations

Brief summary

The cerebral arteriovenous malformations correspond to the formation of an entanglement of morphologically abnormal vessels called nidus, which shunt the blood circulation directly from the arterial circulation to the venous circulation. The cerebral arteriovenous malformations are an important cause of hemorrhagic stroke. The hypothesis is that cerebral haemorrhage associated with a cerebral arteriovenous malformations would come from peri-nidal micro-vessels, in connection with infiltration of leucocytes and / or defective maintenance of microvascular integrity by platelets.

Interventions

None listed

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to No maximum

Inclusion criteria

* Patient over 18 years old * Patient with a cerebral AVM for which an intervention (endovascular treatment or surgery) or only clinical monitoring * Express consent to participate in the study And * children * Free informed and express consent of both holders of the minor patient's parental authority, or, by way of derogation and only if the other holder of parental authority cannot give his or her consent within a time limit compatible with the methodological requirements specific to the conduct of the research with regard to its purposes, of one of the two holders of parental authority

Exclusion criteria

* Patient benefiting from a legal protection measure * Pregnant or breast feeding woman

Design outcomes

Primary

MeasureTime frameDescription
Associaton between dosage of endothelial marker and the arteriovenous malformation pronostic6 monthsassociaton between dosage of endothelial marker in blood samples and correlation with clinical outcome
Associaton between dosage of platelet and the arteriovenous malformation pronostic6 monthsDosage of platelet in blood samples and correlation with clinical outcome
Associaton between dosage of neutrophilic and the arteriovenous malformation pronostic6 monthsDosage of neutrophilic in blood samples and correlation with clinical outcome
Associaton between neo-angiogenesis activation markers and the arteriovenous malformation pronostic6 monthsDosage neo-angiogenesis activation markers in blood samples and correlation with clinical outcome

Countries

France

Contacts

Primary ContactAmélie Yavchitz
ayavchitz@for.paris01 48 63 64 54
Backup ContactJean Philippe DESILLES
jp.desilles@for.paris

Outcome results

None listed

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