Endovascular aortic repair
DeviceTreatment with Gore Endovascular Aortic Products.
NCT Number: NCT01658787
Prospective, observational Registry to obtain data on device performance and clinical outcomes.
This study is active but is not currently recruiting participants.
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Observational
Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia
This is a prospective observational cohort Registry designed to obtain data on device performance and clinical outcomes of patients treated with Gore Endovascular Aortic products.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Treatment with Gore Endovascular Aortic Products.
Time frame: Up to 10 years
W.L.Gore & Associates
Industry
'GREAT' Global Registry for Endovascular Aortic Treatment - Outcomes Evaluation
Acronym: GREAT
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.