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FRED and FRED JR Devices for Intracranial Aneurysm Treatment

M

MicroVention

Status

Completed

Conditions

Intracranial Aneurysm

Treatments

Device: FRED and FRED JR

Study type

Observational

Funder types

Industry

Identifiers

NCT04315168
FRED-EPI

Details and patient eligibility

About

A French, multicenter, prospective, observational, "real-world" assessment of the safety and efficacy of FRED and FRED Jr devices in the treatment of intracranial aneurysms

Full description

Post Market Clinical Follow-up. Multicenter observational study. Treatment and follow-up far at least 12 months as per standard of care.

Sample Size: 138 patients.

Enrollment

135 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with an intracranial aneurysm for which an endovascular treatment is indicated with the device FRED or FRED JR
  • Patient or patient's legally authorized representative has been informed about the study and does not oppose the collection of his/her personal data

Exclusion criteria

  • None

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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