Innovative NeurovaScular Product surveIllance REgistry (INSPIRE)
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Intracranial Ica Aneurysm
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Age: Between 18 - 100 Years
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Gender: Male or Female
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Other Inclusion Criteria:
Neurovascular PSR Registry:- Patient or legally authorized representative (LAR) provides authorization and written informed consent
- 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 or legally authorized representative (LAR) provides authorization and written informed consent and agrees to comply with the study procedures
- Patient has already been selected for endovascular treatment of the target aneurysm with the Pipeline™ Shield Device as the appropriate treatment
You may not be eligible for this study if the following are true:
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Neurovascular PSR Registry:
- Patient who is, or is expected to be, inaccessible for follow-up
- Patient is currently enrolled in, or plans to enroll in, any concurrent drug/device study that may confound the PSR results
- Patient is contraindicated for the device or procedure per the Pipeline™ Shield Device IFU
- The Investigator determined that the health of the patient may be compromised by the patient’s enrollment
- Patient is enrolled or planning to participate in a potentially confounding drug or device trial during the course of this study. Co-enrollment in concurrent
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.