
FRED™ Flow Diverter
Poland: The evaluation of the flow re-direction endoluminal device (FRED™) for the treatment of selected intracranial aneurysms: a Polish multicenter study
"This study offers a comprehensive overview of the flow diversion treatment approach, demonstrating that the FRED™ device is effective and safe for use in intracranial aneurysm treatment. These results align with existing literature, reaffirming the device reliability and suitability for clinical use."
- Patients
86
- Country
Poland
- Clinical Centers
8
- Design
Single arm prospective
- Scope
Patients 18-80 y.o. with unruptured saccular or fusiform intracranial aneurysms located in the anterior circulation (ICA segments C2–C6) or in the posterior circulation (above the PICA).
- Purpose
To evaluate the safety and effectiveness of the FRED™ in the treatment of selected types and location of intracranial aneurysms throughout the complete follow-up period of 24 months.
Endpoints
Effectiveness: Percentage of aneurysms successfully isolated from the rest of the circulation (Grade 4) and patency of the flow-diverter lumen (> 50%: Grade C and D) at 6-, 12- and 24-months of follow-up.
Safety: Rate of clinical complications, including early thromboembolic complications (within the first 3 months), late thromboembolic complications (between 3 and 24 months) and/or hemorrhage from the treated aneurysm, as adjudicated by the Clinical Event Committee.
Efficacy results
At 6 months:
Complete occlusion without parent artery stenosis: 61.8%
Complete occlusion: 64.9%
At 12 months:
Complete occlusion without parent artery stenosis: 76.1%
Complete occlusion: 79.5 %
At 24 months:
Complete occlusion without parent artery stenosis: 82.5%
Complete occlusion: 85.5 %
Safety results
At 24 months:
Clinical complications classified by the CEC as early thromboembolic complication, late thromboembolic complication or hemorrhage from the treated aneurysm: 10.8%
Permanent neurological morbidity: 3.6%
All-cause mortality: 3.6% (including 2.4% of neurological death)
LINK TO STUDY PAGE: PMID: 39984615
Please refer to IFU for the full list of risks, contraindications, warnings, and precautions.

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