HUD -Neuroform

  • STATUS
    Recruiting
Updated on 8 November 2020

Summary

HUD -Neuroform

Description

The Neuroform microdelivery stent is a recently developed product that may be of use in treating intracranial wide-necked aneurysms. The Neuroform stent can be placed in a brain artery across the opening of an aneurysm. The coils prevent blood from flowing into the aneurysm and could greatly reduce the risk of aneurysm rupture. The Neuroform stent is a small metallic mesh tube that is designed to keep the coils in the aneurysm sac.

Patient Inclusion Criteria: Adults scheduled at the hospital to undergo an endovascular treatment of the aneurysm. Every patient suffering from an un-ruptured or ruptured aneurysm, for whom the endovascular treatment approach using the Neuroform3TM stent is considered by the therapeutic team in charge.

Details
Condition Aneurysm
Clinical Study IdentifierTX135528
Last Modified on8 November 2020

Eligibility

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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