Loading clinical trials...
Loading clinical trials...
ARCHYTAS: AAA Registry: Clinical Outcomes of Highly Angulated anatomY Treated With the Aorfix™ Stent Graft
The ARCHYTAS Registry is a long-term, global, multicenter, non-randomized, prospective, registry designed to collect "on-label" data in real world clinical settings on patients undergoing endovascular repair with the latest generation Aorfix™ AAA Flexible Stent Graft System. Registry data will augment existing data from ongoing and prospective Aorfix™ clinical trials for the purposes of publication, general product development and quality measures.
The ARCHYTAS Registry is a long-term, global, multicenter, non-randomized, prospective, registry established by Lombard Medical Ltd. (Lombard) to collect "on-label" data in real world clinical settings on patients undergoing endovascular repair with the latest generation Aorfix™ AAA Flexible Stent Graft System, for treatment of abdominal aortic and aorto-iliac aneurysms in anatomy where the aorta in the aneurysm neck is bent through an angle between 0° and 90°. This indication for Aorfix™ is approved in all territories where this Registry is being operated and this Registry does not seek to collect data on any use of the implant for which full commercial approval does not already exist. The ARCHYTAS Registry data will augment existing data from ongoing and prospective clinical trials with Aorfix™ for the purposes of publication, general product development and quality measures.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Prague University Hospital
Prague, Czechia
Charité - Universitätsmedizin Berlin
Berlin, Germany
Universitätsklinikum Herzzentrum Köln
Cologne, Germany
Alfried Krupp Krankenhaus
Essen, Germany
Elisabeth-Krankenhaus Essen
Essen, Germany
Universitätsklinikum Frankfurt
Frankfurt, Germany
University Hospital Halle
Halle, Germany
Universitätsklinikum Leipzig
Leipzig, Germany
St.Vincenz-Krankenhaus Limburg
Limburg, Germany
Bonifatius Hospital
Lingen, Germany
Start Date
April 1, 2015
Primary Completion Date
April 1, 2022
Completion Date
April 1, 2022
Last Updated
November 1, 2021
500
ESTIMATED participants
Stent Graft
DEVICE
Lead Sponsor
Lombard Medical
NCT07184723
NCT06710938
NCT06884397
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions