Physician-Sponsored IDE for Talent Endoluminal Spring Graft System in Patients With AAA
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 49
- 试验地点
- 2
- 主要终点
- Number of Participants With Successful Exclusion of Abdominal Aortic Aneurysm
研究概览
简要总结
The purpose of this study is to evaluate the safety and effectiveness of the Talent Endoluminal Spring Graft System, an investigational device, to treat abdominal aortic aneurysms (AAA). The treatment population will include patients with an abdominal aortic aneurysm who meet the inclusion/exclusion criteria. All patients in the treatment population will undergo post-procedure follow-up evaluations at one (1), six (6), and 12 months and annually thereafter up to five (5) years post-procedure.
详细描述
Endovascular aneurysm repair (EVAR) offers certain advantages as compared to surgical repair of an abdominal aortic aneurysm. Known benefits associated with EVAR, as described in scientific literature, include minimally invasive procedure, shorter ICU and hospital stay, reduced blood loss, more rapid recovery, and reduced need for general anesthesia. Potential benefits that may be associated with use of the Talent device include reduced occurrence of endoleaks, therefore reduced subsequent re-interventions. The risks/complications known to occur to all patients undergoing AAA repair may include anesthetic complications, (e.g., aspiration), aneurysm enlargement, rupture, perforation or dissection, bleeding, arterial or venous thrombosis and/or pseudoaneurysm, arteriovenous fistula, hematoma or coagulopathy, bowel complications, cardiac complications, (e.g., arrhythmia, myocardial infarction, congestive heart failure, hypotension, hypertension), embolization (micro and macro) with transient or permanent ischemia or infarction, genitourinary complications, infection, neurologic complications, occlusion of device or native vessel, pulmonary/respiratory complications and renal complications.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects who participate in this study must fulfill all of the following criteria.
- •Subject is > 18 years of age.
- •Subject is not pregnant, and, if female and of child-bearing potential, is practicing contraception.
- •Subject has documented evidence of at least one patent internal iliac artery.
- •Subject has an AAA that is dilated to > 4 cm in diameter.
- •Subject has a proximal AAA neck (distance between the top of the aneurysm and the renal arteries) > 5 mm.
- •Subject has a proximal aortic neck diameter > 14 mm and < 32 mm.
- •Subject has an angle between the suprarenal aorta and the aneurysm <60o.
- •Subject has renal arteries > 9 cm from the aortic bifurcation.
- •Subject has proximal and distal iliac neck diameters > 8 mm and < 18 mm to accommodate stock devices. For those subjects whose proximal and distal iliac diameters are > 18 mm, custom devices with a variation in fixation diameters will be ordered from the manufacturer.
- •Subject has a distal iliac neck length > 15 mm.
- •Subject has signed informed consent.
- •Subject will be available for follow-up for 12 months after the procedure.
排除标准
- •Subjects who fulfill any of the following criteria may not participate in this study.
- •Subject has patent internal iliac arteries that require graft extension to the external iliac arteries.
- •Subject has one or more patent subrenal arteries with potential retrograde flow after stent-grafting.
- •Subject has a dominant patent inferior mesenteric artery and an occluded or stenotic celiac and superior mesenteric artery.
- •Subject has an aneurysm involving both internal iliac arteries.
- •Subject has a lesion that cannot be crossed with a guide wire.
- •Subject whose arterial access site cannot accommodate the delivery catheter.
- •Subject has no distal vascular bed.
- •Subject has systemic infection, or is suspected of having systemic infection.
- •Subject has contraindications for use of contrast medium or anticoagulation drugs.
- •Subject has received a previous stent in the subrenal aorta.
- •Subject has an untreatable bleeding diathesis.
- •Subject is in a hypercoagulable state.
结局指标
主要结局
Number of Participants With Successful Exclusion of Abdominal Aortic Aneurysm
时间窗: From the date of treatment assessed up to 5 years post treatment.
The safety and effectiveness of the endoluminal device was determined by the number participants with successful exclusion of the abdominal aortic aneurysm (AAA).
次要结局
- Number of Participants With Successful Device Delivery and Deployment(From the date of treatment assessed up to 5 years post treatment.)
研究者
Rodney A. White, M.D.
Chief, Vascular Surgery
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center