NCT01960491已完成不适用
Prospective Single Center Pilot Clinical Study to Evaluate the Safety and Effectiveness of an Intracardiac Septal Closure Device With Biodegradable Framework in Patients With Clinically Significant Atrial Septum Defect (ASD) or Patent Foramen Ovale (PFO)
Carag AG1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2014年5月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Effective closure of defect
研究概览
简要总结
The objective of this study is to evaluate the effectiveness and the safety of the intracardiac septal closure device (CBO), as well as the practicability of implantation of this device using the accessories (DS for CBO).
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
- •Age greater than 18 years - no upper limit of age
- •Body weight > 40 kg
- •Patients with an isolated ASD or PFO determined as suitable for closure via a commercially available device
- •In ASD patients, echocardiographic evidence of right ventricular overload, and a stretched diameter of the defect up to 25 mm
- •In patients with PFO, echocardiographic evidence of right to left shunt, and intraatrial tunnel length up to 4 mm
- •Signed informed consent, respectively ability to give written informed consent after being told of the potential benefits and risks of entering the trial
- •For female patients of child bearing capacity: Exclusion of pregnancy before start of the study and willingness to use adequate contraceptive methods to prevent pregnancy during the study
排除标准
- •ASD/PFO larger than a stretched diameter of 25 mm, or defects unsuitable for percutaneous closure
- •Intraatrial tunnel longer than 4 mm
- •Multiple or fenestrated ASD, ostium primum or sinus venosus atrial septal defect, coronary sinus defect
- •Any significant cardiac valve dysfunction
- •Anomalous pulmonary veins
- •Defects with inadequate margins, as is consistent with current standards of care, such that the device will not position appropriately so as to avoid interference with other cardiac structure, or that will subject the device to increased risk of embolization post deployment.
- •Acquired pathological or congenital deficiencies of the cardiovascular system (any other than ASD; e.g. transposition of vessels, calcification, myocardial infarction, intracardiac thrombi), being clinically significant, respectively interfering in the investigator's opinion with the conduct of study
- •Clinically significant dilated cardiomyopathy (paroxysmal or caused by e.g. myocarditis or other reasons)
- •Any patient known to have extensive or complex congenital cardiac anomaly which can only be adequately repaired by way of cardiac surgery
- •Echocardiographic evidence of thrombus in the left atrium, left atrial appendage, or other cardiac chamber, and in the inferior vena cava.
- •Patients who within one month prior to implantation are known to have sepsis or any systemic infection that has not been successfully treated prior to device placement
- •Active endocarditis or other infections producing bacteremia.
- •Clinically relevant arrhythmia
- •Patients whose vasculature, through which access to the defect is gained, is inadequate to accommodate the size of the device, the position controls or the introduction sheath
- •Documented history of bleeding, clotting or coagulation disorders, untreated ulcer or any other contraindications to acetylsalicylic acid therapy, unless another anti-platelet agent can be administered for 6 months
- •Known hypercoagulable state
- •Anamnesis respectively diagnosis of pregnancy, or breastfeeding patients
- •Any disorder in the investigator's opinion that could interfere with compliance or safety evaluation as well as any severe concurrent illness that would limit life expectancy (e.g. malignancies)
- •Participation in an investigational drug or device trial within 30 days prior to selection (day 0) or current inclusion in any other clinical trial or research project
- •Subjects who, in the opinion of the investigator, will be inappropriate for inclusion into this clinical trial or will not comply with requirements of the study
- •Patients who are kept lawfully in an institution
- •Clinical investigations shall be conducted in vulnerable populations only when they cannot be carried out in non-vulnerable populations and shall follow the additional ethics committee procedures where applicable. These clinical investigations shall be designed specifically to address health problems that occur in the vulnerable population, and offer the possibility of direct health-related benefit to the vulnerable population
结局指标
主要结局
Effective closure of defect
时间窗: 6 months
次要结局
未报告次要终点
研究者
研究点 (1)
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