NCT02703428已完成不适用
The LUCY Study: TriVascular Evaluation of Females Who Are Underrepresented Candidates for Abdominal Aortic Aneurysm Repair in Europe
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
- 试验地点
- 10
- 主要终点
- Freedom from access-related vascular complications and freedom from AAA-related mortality through 30 days.
研究概览
简要总结
The LUCY Study is a prospective, consecutively enrolling, non-randomized multi center post-market study to evaluate the low profile (14F) Ovation® Abdominal Stent Graft Platform when used in the endovascular treatment of female patients.
详细描述
The LUCY Study is a prospective, consecutively enrolling, non-randomized multi center post-market study to evaluate the Ovation Abdominal Platform when used in the endovascular treatment of female patients.
The primary endpoint is freedom from access-related vascular complications and freedom from AAA-related mortality through 30 days.
Secondary endpoints of the study will be achieved by demonstrating the benefits in female patients despite the fact that historically fewer female patients have been eligible for EVAR, and they have experienced a higher rate of access-related complications and higher mortality rates. Secondary endpoints will be evaluated through 1 year (365 ± 60 days) post-procedure.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Patient is > 18 years of age.
- •Patients who are non-pregnant female (females of child bearing potential must have a negative pregnancy test prior to enrollment into the study).
- •Patient has signed an Ethics Committee (EC) approved Informed Consent Form.
- •Patient is considered by the treating physician to be a candidate for elective open surgical repair of the AAA (i.e., category I, II, or III per American Society of Anesthesiology (ASA) classification). ASA category IV patients may be enrolled provided their life expectancy is greater than 1 year.
- •Patient has an infrarenal abdominal aortic aneurysm that meets at least one of the following:
- •Abdominal aortic aneurysm >5.0 cm in diameter;
- •Aneurysm has increased in size by 0.5 cm in last 6 months; or
- •Maximum diameter of aneurysm exceeds 1.5 times the transverse dimension of an adjacent non-aneurysmal aortic segment.
- •Patient has suitable anatomy that allows use of the TriVascular Ovation Abdominal Platform:
- •Iliac or femoral arteries that allow endovascular access with the TriVascular Ovation Abdominal Platform.
- •Proximal aortic neck landing zone with an inner wall diameter of no less than 16 mm and no greater than 30 mm at 13 mm below the inferior renal artery.
- •Distal iliac artery landing zone length (seal zone) of ≥10 mm. The resultant repair should preserve patency in at least one hypogastric artery.
- •Distal iliac artery landing zone an inner wall diameter of no less than 8 mm and no greater than 25 mm.
- •Distance from the most distal renal artery to most superior internal iliac artery measurement is at least 130 mm.
- •Aortic angle of ≤ 60 degrees if proximal neck length is ≥10 mm and ≤ 45 degrees if proximal neck length is <10 mm.
- •Patient must be willing to comply with all required follow-up exams.
排除标准
- •Patient has a need for emergent surgery.
- •Patient has a dissecting aneurysm.
- •Patient has an acutely ruptured aneurysm.
- •Patient has an acute vascular injury.
- •Patient has had a previous repair of the abdominal aortic aneurysm or an iliac artery in intended treatment zone.
- •Patient has a known thoracic aortic aneurysm or dissection that will require treatment (surgery or endovascular intervention) within the study period.
- •Patient has a mycotic aneurysm or has an active systemic infection.
- •Patient has unstable angina (defined as angina with a progressive increase in symptoms, new onset at rest or nocturnal angina, or onset of prolonged angina).
- •Patient has had a myocardial infarction (MI) and/or stroke (CVA) within the past 6 months.
- •Patient requires use of techniques (e.g. Chimney graft) that would cover the renal arteries.
- •Patient requires planned adjunctive devices (e.g. renal stents) to complete the procedure.
- •Patient has a major surgical or interventional procedure planned during or within ±30 days of the AAA repair.
- •Patient has history of connective tissue disease (e.g., Marfan's or Ehler's-Danlos syndrome).
- •Patient has history of bleeding disorders or refuses blood transfusions.
- •Patient has dialysis dependent renal failure or baseline serum creatinine level >2.0 mg/dl
- •Patient has a known hypersensitivity or contraindication to anticoagulation or contrast media that is not amenable to pre-treatment.
- •Patient has a known allergy or intolerance to polytetrafluoroethylene (PTFE), PEG-based polymers, fluorinated ethylene propylene (FEP) or nitinol.
- •Patient has a body habitus that would inhibit X-ray visualization of the aorta.
- •Patient has a limited life expectancy of less than 1 year.
- •Patient is currently participating in an investigational device or drug clinical trial.
- •Patient has other medical, social or psychological conditions that, in the opinion of the investigator, preclude them from receiving the pre-treatment, required treatment, and post-treatment procedures and evaluations.
结局指标
主要结局
Freedom from access-related vascular complications and freedom from AAA-related mortality through 30 days.
时间窗: 30 ± 10 days
次要结局
- Serious and Non-Serious Adverse Events(365 ± 60 days)
- Access-related vascular complications(365 ± 60 days)
- Freedom from conversion to open repair(365 ± 60 days)
- Freedom from Abdominal Aortic Aneurysm rupture(365 ± 60 days)
- Freedom from Type I & III endoleaks(365 ± 60 days)
- Length of hospital and ICU (if required)(365 ± 60 days)
- Anesthesia Type(365 ± 60 days)
- Freedom from migration(365 ± 60 days)
- Technical (deployment) success(365 ± 60 days)
- Freedom from aneurysm enlargement(365 ± 60 days)
- Freedom from AAA related secondary interventions(365 ± 60 days)
- Freedom from mortality (all cause and AAA related)(365 ± 60 days)
- Blood Loss(365 ± 60 days)
- Duration of Procedure(365 ± 60 days)
研究者
研究点 (10)
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