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To assess the safety and performance of Aorfix™ Stent Grafts in the treatment of Abdominal Aortic and Aorto-Iliac Aneurysm where a significant degree of vessel angulation exists at the neck of the aneurysm or in the common iliac arteries.
The Aorfix™ Stent Graft is currently a CE-marked product indicated for AAA where the angle of the aneurysm is <65o. The objective of this study is to evaluate the safety and performance of the bifurcated Aorfix™ Stent Graft in the treatment of infrarenal abdominal aortic aneurysms and aorto-iliac aneurysms, in infrarenal necks angulated > 60o (between 60 to 90 degrees) as measured by 3-dimensional reconstruction in order to widen the indication.
The investigation is a prospective open label, single arm, multi-centre clinical study. The study group will consist of 25 evaluable participants. In order to account for patients lost to follow up (estimated at approximately 20%) up to 30 patients will be enrolled in the study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Open label, single arm | Active Comparator | A prospective, open label, single-arm (non-randomized) multi-center, international clinical device investigation to collect safety and performance data concerning the Aorfix™ Stent Graft System in the treatment of abdominal aortic aneurysm and aorto-iliac aneurysm where a significant degree of vessel angulation exists |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Aorfix™ Stent Grafts (AAA endovascular procedure) | Device | Endovascular treatment of AAA using the Aorfix™ Stent Graft and Delivery System |
|
| Measure | Description | Time Frame |
|---|---|---|
| The primary endpoints are acute technical success, initial performance and safety at 1-month follow up. | 1-month post-procedure |
| Measure | Description | Time Frame |
|---|---|---|
| Secondary endpoints will examine recovery factors: operative time, ICU duration, blood loss, days to normal diet, days to discharge, days to ambulation, freedom from non-clinical events, need for secondary procedure and conversion to uni-iliac. | 6-months post-procedure | |
| As well as safety at 6-month follow-up as measured by serious adverse events that occur up to 6-months post-procedure. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| William C Loan, MD, FRCR | Belfast City Hospital Trust, Belfast, Ireland | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| 2 Interni Klinika; General University Hospital | Prague | 12800 | Czechia | |||
| Klinik für Gefäßchirurgie; St.-Franziskus Hospital Münster |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 11013038 | Background | Harris PL, Vallabhaneni SR, Desgranges P, Becquemin JP, van Marrewijk C, Laheij RJ. Incidence and risk factors of late rupture, conversion, and death after endovascular repair of infrarenal aortic aneurysms: the EUROSTAR experience. European Collaborators on Stent/graft techniques for aortic aneurysm repair. J Vasc Surg. 2000 Oct;32(4):739-49. doi: 10.1067/mva.2000.109990. |
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| ID | Term |
|---|---|
| D017544 | Aortic Aneurysm, Abdominal |
| ID | Term |
|---|---|
| D001014 | Aortic Aneurysm |
| D000783 | Aneurysm |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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| 6-months post-procedure |
| Münster |
| 48145 |
| Germany |
| Department of Interventional Radiology, University School of Medicine | Lublin | 20954 | Poland |
| Vascular Surgery Division, Thoracic Institute, Hospital Clinic, University of Barcelona | Barcelona | 08036 | Spain |
| Belfast City Hospital Trust | Belfast | United Kingdom |
| Freeman Hospital; Main X-Ray | Newcastle upon Tyne | NE7 7DN | United Kingdom |
| D001018 |
| Aortic Diseases |