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Interest of New MRI Sequences After Embolization of Brain Arteriovenous Malformations

Interest of New MRI Sequences After Embolization of Brain Arteriovenous Malformations (MAV-IRM)

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02896881
Acronym
MAV-IRM
Enrollment
53
Registered
2016-09-12
Start date
2017-02-01
Completion date
2025-02-03
Last updated
2026-01-22

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

Conditions

Brain Arteriovenous Malformations

Brief summary

In previous studies exploring specific sequences of MRI (susceptibility weighted imaging (SWI) and arterial spin labeling (ASL)), the investigators have shown the great sensibility of these MRI sequences to detect arteriovenous shunts, compared to angiography imaging (static or dynamic). This prospective study aims to compare multisequence MRI to brain arteriography imaging in patients undergoing brain arteriovenous malformations embolization.

Detailed description

Cerebral arteriovenous malformations are treated to eliminate the potential risk of haemorrhage. There are three possible treatment modalities: surgery, radiosurgery or embolisation. Complete exclusion of the arteriovenous malformation is a prerequisite for confirming that there is no residual risk of haemorrhage. After treatment, arteriography is the gold standard for confirming this exclusion. The absence of early opacification of the venous drainage is considered a sign of cure. Several arteriographic aspects are possible after treatment by embolisation: * Arteriography may be strictly normal (no abnormalities). * The persistence of early venous opacification (presence of arterialised blood) indicates the persistence of a residual AVM. * Other vascular anomalies without early venous drainage may be present: dysplastic vessels (irregular shape, "corkscrew" appearance) ; capillary blush in the embolisation bed (hyperaemia) ; other: slow flow, slow filling, or widening of afferent arteries. Our previous studies exploring the use of specific MRI sequences, in magnetic susceptibility (SWI), arterial spin labelling (ASL) and angiography (static or dynamic) sequences, have enabled us to demonstrate the very high sensitivity of these sequences for detecting an arteriovenous shunt, whether native (when the AVM is discovered) or residual after treatment. We would like to carry out a prospective study to compare cerebral arteriography and MRI (multi-sequence) in patients treated by embolisation for cerebral arteriovenous malformation.

Interventions

None listed

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Patient ≥ 18 years old * with brain Arteriovenous Malformations * embolization treatment scheduled

Exclusion criteria

* patient's refusal to participate in the study * contraindication to undergo MRI examination * patient under legal protection

Design outcomes

Primary

MeasureTime frameDescription
sensitivity of multisequence MRI to detect a residual arteriovenous malformation after embolizationwithin 3 months after embolizationEarly opacification of a vein, possibly associated with the presence of abnormal vessels, will be sought, indicating a residual malformation. After interpretation of the MRI (angio-MRI with multi-sequences, magnetic susceptibility (SWI), arterial spin labelling (ASL) and static or dynamic angiography), the result will be coded dichotomously: (presence/absence of a residual malformation). The arteriography result will be coded in the same way. The sensitivity of the new MRI sequences for detecting a residual arteriovenous malformation after treatment by embolisation will thus be assessed, compared with arteriography (gold-standard).

Countries

France

Contacts

PRINCIPAL_INVESTIGATORRaphaël BLANC, MD

Fondation Ophtalmologique Adolphe de Rothschild

Outcome results

None listed

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