Actively Recruiting
NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study
Led by Medtronic Neurovascular Clinical Affairs · Updated on 2026-04-02
118
Participants Needed
4
Research Sites
402 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of the Pipeline™ Vantage Embolization Device with Shield Technology™ Post Approval Study (PAS) ("Pipeline™ Vantage PAS") is to collect safety and effectiveness data in patients undergoing treatment for intracranial aneurysms (IA) using the Pipeline™ Vantage Embolization Device with Shield Technology™ ("Pipeline™ Vantage Device") in a post approval setting.
CONDITIONS
Official Title
NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient or legally authorized representative has provided written informed consent and agrees to comply with study requirements.
- Patient has an intracranial aneurysm intended for treatment with the Pipeline17 Vantage Embolization Device with Shield Technology.
- Patient is an adult according to local law at time of consent.
You will not qualify if you...
- Patient has any contraindications for the device or procedure as per local instructions for use.
- Patient may be unable to complete study follow-up.
- Investigator believes the patient's health may be compromised by study enrollment.
- Female patient is pregnant, breastfeeding, or planning pregnancy during the study.
- Patient is currently enrolled in or plans to enroll in another drug or device study that could affect results.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
Wellstar Research Institute
Marietta, Georgia, United States, 30060
Actively Recruiting
2
University of Iowa Hospitals and Clinics
Iowa City, Iowa, United States, 52242
Actively Recruiting
3
McLaren Healthcare
Flint, Michigan, United States, 48532
Actively Recruiting
4
Semmes Murphey Clinic/Semmes Murphy Foundation
Memphis, Tennessee, United States, 38120
Actively Recruiting
Research Team
M
Medtronic Neurovascular Clinical Affairs
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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