Health Trials

Clinical trials

4

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck Bifurcating Intracranial Aneurysms (IAs).

The purpose of this study is to assess the safety and effectiveness of the Artisse™ Intrasaccular Device in the treatment of unruptured and ruptured wide-neck bifurcating intracranial aneurysms.

Participants needed: 300
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Medtronic Neurovascular Clinical AffairsUpdated: Jun 30, 2026Locations: 22
Eligibility criteria

Subject or subject's Legally Authorized Representative (LAR) has provided writte... [+11]

During treatment planning, it is determined that subject may need an adjunctive... [+12]

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Status: Recruiting

NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study

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.

Participants needed: 118
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: Medtronic Neurovascular Clinical AffairsUpdated: Jun 23, 2026Locations: 7Duration: 5 Years
Eligibility criteria

Patient or legally authorized representative (LAR) has provided written informed... [+2]

Patient with any contraindications for the device or procedure per the Pipeline™... [+4]

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Participants needed: 1,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Medtronic Neurovascular Clinical AffairsUpdated: Jun 18, 2026Locations: 1Duration: 90 Days
Eligibility criteria

Patient or legally authorized representative (LAR) provides authorization and/or... [+2]

Participant who may be unable to complete follow-up within the registry. [+2]

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Status: Recruiting

Neurovascular Product Surveillance Registry

Post market surveillance registry

Participants needed: 4,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Medtronic Neurovascular Clinical AffairsUpdated: Jun 2, 2026Locations: 99Duration: 5 Years
Eligibility criteria

Patient or legally authorized representative (LAR) provides authorization and/or... [+3]

Patient who is, or is expected to be inaccessible for follow-up [+10]

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