A Continuation Study of the AeriSeal® System Administered at 3 to 4 Sites During a Single Treatment Session for Lung Volume Reduction in Patients With Advanced Emphysema
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 发起方
- 入组人数
- 18
- 试验地点
- 4
- 主要终点
- Change from baseline in Percent Volume of Lung
研究概览
简要总结
The purpose of this study is to assess the long term safety and efficacy of AeriSeal System treatment administered at up to 4 subsegments during a single treatment session for lung volume reduction in patients with advanced emphysema through 48 weeks after treatment.
详细描述
Emphysema is a progressive, debilitating disease characterized by destruction of lung tissue as a result of inflammation caused by exposure to noxious inhaled agents for extended periods. The most common cause of this condition is cigarette smoking, although genetic, occupational, and environmental causes account for up to 10% of cases. Despite aggressive public health initiatives aimed at discouraging the use of cigarettes, smoking-related lung diseases remain a significant cause of disability and death worldwide. Due to the number of current and new smokers, emphysema is expected to remain a leading cause of morbidity and mortality for years to come.
The AeriSeal System is a novel device system being developed for the treatment of advanced emphysema. The AeriSeal System is administered bronchoscopically, and designed to provide the physiological benefits of lung volume reduction without the risks and cost of major surgery.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 40 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients must have been enrolled in the 03-C10-002PLV Aeris' Investigational Study and completed a minimum of 12 weeks of follow-up following AeriSeal System treatment.
排除标准
- 未提供
结局指标
主要结局
Change from baseline in Percent Volume of Lung
时间窗: 48 Weeks following treatment
Computed Tomography (CT) evidence of lobar volume reduction at site(s) of AeriSeal Foam Sealant administration at 48 weeks post treatment, assessed quantitatively by digital integration of CT dicom images collected using a standardized image acquisition and reconstruction algorithm.
次要结局
- Change in Forced Expiratory Volume in 1 Second (FEV1)(24 and 48 weeks following treatment)
- Change in distance walked in six minutes(24 and 48 weeks following treatment)
- Change in the ratio of Residual Volume (RV) to Total Lung Capacity (TLC)(24 and 48 weeks following treatment)
- Change in Forced Vital Capacity (FVC)(24 and 48 weeks following treatment)
- Change in St. George's Respiratory Questionnaire (SGRQ)domain score(24 and 48 weeks following treatment)
- Change in Medical Research Council Dyspnea (MRCD) score(24 and 48 weeks following treatment)