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Study identifier: NCT06940934 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Post-Market Product Surveillance of Intracranial ANeurysms Treated With Commercial ReGistered ACANDIS Devices in FrancE

Condition: Intracranial Aneurysms  ·  Sponsor: Acandis GmbH

PhaseN/A
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The aims of this clinical data collection are to investigate mortality, morbidity and neurological outcome 12 months after treatment of subject's intracranial aneurysm(s) and additionally to evaluate potential residual risks associated with the use of the commercial device(s) and to ensure the long-term safety and performance of Acandis Device(s) after its placing on the French market. On top of this, these cohorts will generate data for getting the renewal of the device's reimbursement on the French market.

This description comes directly from the study's public registry record.

Talk to the study team

Acandis GmbH  ·  +49 7231 980 84 0  ·  clinicalaffairs@acandis.com

Always discuss trial participation with your own doctor first.

Locations (1)

Neuroradiologie Interventionnelle, CHU de Rouen (Charles Nicolle)Rouen, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06940934