Neurovascular Product Surveillance Registry

  • STATUS
    Recruiting
  • End date
    Nov 16, 2026
  • participants needed
    3000
  • sponsor
    Medtronic Neurovascular Clinical Affairs
Updated on 16 June 2021
stroke
embolization procedure

Summary

Post market surveillance registry

Description

An observational, prospective, multi-center, single-arm registry to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic Neurovascular market-released products used in the treatment of Intracranial aneurysms and Acute Ischemic Stroke.

Details
Condition Berry Aneurysm, Aneurysm, Ischemic Stroke, Stroke Ischemic, intracranial aneurysm
Treatment Treatment for intracranial aneurysms, Treatment for Acute Ischemic Stroke
Clinical Study IdentifierNCT02988128
SponsorMedtronic Neurovascular Clinical Affairs
Last Modified on16 June 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patient or legally authorized representative (LAR) provides authorization and/or consent per institution and geographical requirements
Patient has, or is intended to receive or be treated with, an eligible Medtronic product
Patient is consented within the enrollment window of the therapy received, as applicable
Patient is at least 18 years of age at time of enrollment

Exclusion Criteria

Patient who is, or is expected to be inaccessible for follow-up
Patient with exclusion criteria required by local law
Patient is currently enrolled in or plans to enroll in any concurrent drug and/or device study that may confound results
Female patient who is known to be pregnant or is breastfeeding or wishes to become pregnant during participation in the study
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  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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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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