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Principal Investigator left the organization and took the IDE/Study with him
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This trial evaluates surgeon-modified fenestrated-branched stent-grafts (sm-FBSG) for Abdominal Aortic Aneurysms (AAA) that are custom-made intra-operatively with no waiting period by a qualified vascular surgeon. In addition, it aims to examine the alternative sm-FBSG for patients with restricted access to centers performing clinical trials with commercially available devices and those patients with aortic emergencies.
Complex aortic aneurysms are those involving the renal and visceral arteries, and open repair of these aneurysms requires more extensive dissection, aortic clamping above the renal or mesenteric arteries, and possible reconstruction of aortic branches. Recovery time tends to be longer, including more hospital days, than for endovascular repair, and there is a greater potential for complications. Many high-risk patients with aneurysms of the abdominal aorta (AAA), including thoracoabdominal aortic aneurysms (TAAA), and significant co-morbidities will be denied elective open surgery because of heightened risks associated with open repair of complex aneurysms, and therefore, the potential benefit of an endovascular option increases as well.
Endovascular aneurysm repair has been shown to be an effective alternative in treating uncomplicated infrarenal and thoracic aneurysms in both the elective and urgent setting, yet there is limited experience with this technology in complex conditions. Fenestrated grafts have been developed as a minimally invasive treatment for patients with complex aortic aneurysms who are unfit for traditional open surgery.
Surgeon-modified fenestrated-branch stent grafts (sm-FBSG) with branches for the visceral vessels are custom-made by a qualified vascular surgeon for patients with complex aortic conditions. It is expected that they will minimize surgical risks and promote quicker recovery, and they could represent a therapeutic option for high-risk patients unfit for open surgery.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| surgeon-modified fenestrated-branched stent-grafts (sm-FBSG) | Other |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| surgeon-modified fenestrated-branched stent-grafts (sm-FBSG) | Device |
|
| Measure | Description | Time Frame |
|---|---|---|
| Determine the safety and effectiveness of sm-FBSG for the treatment of complex aortic aneurysms in patients at high-risk for open surgical repair. | Major adverse events defined as:
The primary effectiveness endpoint is the proportion of treatment group subjects that achieve treatment success. Treatment success is a composite endpoint assessed at 12 months that includes successful delivery and deployment of the graft with branch vessel preservation (technical success) as well as freedom from Type 1 and 3 endoleaks, graft migration, and AAA enlargement or rupture. Technical success is defined as successful delivery and deployment of the physician modified endovascular graft with preservation of those branch vessels intended to be preserved. Includes freedom from the following at 12 months: Type I & III endoleak, stent graft migration, AAA enlargement, AAA rupture and conversion to open repair through 12 months. | 30 Days |
| Measure | Description | Time Frame |
|---|---|---|
| Evaluate postoperative all-cause morbidity after repair with sm-FBSG |
| >30 Days to 5 Years |
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Inclusion Criteria (abbreviated):
Exclusion Criteria (abbreviated):
Anatomic exclusion criteria: iliac arteries and aorta must be able to accommodate endovascular devices and procedure
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| Name | Affiliation | Role |
|---|---|---|
| Joseph J. Ricotta, II, MD, MS, FACS | Northside Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Northside Hospital | Atlanta | Georgia | 30342 | United States |
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| Label | URL |
|---|---|
| Northside Vascular Website | View source |
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| ID | Term |
|---|---|
| D000783 | Aneurysm |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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| Evaluate long-term survival and complications after repair of complex aortic aneurysms with sm-FBSG |
|
| >30 Days to 5 Years |
| Successful device delivery and deployment with patency of all branches |
| 30 Days, 3 Months, 6 Months, and Years 1 to 5 |
| Procedural / In-Hospital Evaluations |
| 30 Days |