Intervascular Post-Market Clinical Follow-Up (PMCF) Registry

Recruiting Observational Study
Carotid Artery Diseases Aortic Diseases Peripheral Arterial Diseases
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
1,200 (estimated)
Sponsor
Intervascular · Industry
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About This Trial
The purpose of this registry is to evaluate the long-term safety and performance of Intervascular Vascular Grafts and Patches (Intergard Standard, Hemashield, Intergard Silver, Intergard Synergy) for bypass, repair or replacement of aortic, peripheral, or carotid arteries. This registry is intended to further define the expected product lifetime of the devices and to collect data related to useful…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Willing, and able to provide legally-effective written informed consent (as required by Institutional Review Board or Ethics Committee) * Male and female patients that have undergone bypass, replacement or repair of the peripheral arteries, aorta, or carotid artery using the I…
Contacts

Senior Manager, Clinical Affairs

+1 603 233 7685

kristen.nolin@getinge.com

CONTACT