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RECRUITING
NCT07748572

PMCF Registry to Describe the Safety and Performance of p64, p48 MW and p64 MW in France

Sponsor: Phenox GmbH

View on ClinicalTrials.gov

Summary

To evaluate safety and performance of the phenox GmbH Flow Diverter p64, p64 MW, and p48MW in France, this registry will include subjects with intracranial aneurysms (anterior and posterior) who are treated with a phenox GmbH Flow Diverter. The subjects will be treated according to the standard of care in the participating sites.

Official title: CEFloW (Clinical Experience With Flow Diverter With and Without Movable Wire)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2025-03-07

Completion Date

2028-12

Last Updated

2026-08-05

Healthy Volunteers

No

Interventions

DEVICE

Aneurysm treatment with a Flow Modulation Device

Treatment of an intracranial aneurysm (anterior and posterior circulation) with a p64, p48 MW, or p64 MW Flow Modulation Device.

Locations (11)

CHU Amiens-Picardie

Amiens, France

CHU Bordeaux

Bordeaux, France

CHU Pierre Wertheimer

Bron, France

CHU Clermont-Ferrand

Clermont-Ferrand, France

Hôpital Bicêtre

Le Kremlin-Bicêtre, France

CHU de Limoges

Limoges, France

Hôpital Pitié-Salpêtrière

Paris, France

CHU Reims

Reims, France

CHU Rouen

Rouen, France

CHRU Strasbourg

Strasbourg, France

CHU Tours

Tours, France