Effect of Noninvasive Positive Pressure Ventilation on Pulmonary Function Testing in Amyotrophic Lateral Sclerosis
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 8
- 试验地点
- 1
- 主要终点
- Difference in Pulmonary Function and Respiratory Muscle Pressure Testing
研究概览
简要总结
Amyotrophic Lateral Sclerosis (ALS), or "Lou Gehrig's Disease", is a fatal disorder that causes progressive degeneration and weakening of the muscles of breathing, leading to breathing insufficiency and eventually breathing failure. This breathing insufficiency is commonly treated with a breathing assistance device, known as noninvasive positive pressure ventilation (NIPPV). While generally well tolerated and accepted, it is not clear whether or to what extent NIPPV in fact helps breathing function: some data suggest that NIPPV preserves breathing function over time, whereas other data suggest that it actually causes breathing function to decline more quickly. No studies have shown what the acute effect of NIPPV is on breathing muscle function in ALS patients.
This study will test the hypothesis that the acute use of NIPPV, at pressure levels that are in common clinical use, will cause measurable changes in tests of breathing function, compared to baseline and to lower levels of NIPPV. We expect that the results of this study will help to clarify whether and to what extent NIPPV assists respiratory muscle function in patients with ALS.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Supportive Care
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •clinical diagnosis of amyotrophic lateral sclerosis
- •clinical indication to start noninvasive ventilation (forced vital capacity < 50% predicted or signs/symptoms of respiratory insufficiency)
- •age 18 to 80 years old
排除标准
- •prior institution of NIPPV
- •inability to safely use NIPPV
- •indications for tracheostomy assisted ventilation because of inability to clear secretions from the airway
- •inability or unwillingness to perform pulmonary function testing
- •presence of advanced dementia.
研究组 & 干预措施
High-level ventilation
Each subject will spend 2 hours receiving high-level noninvasive ventilation.
干预措施: noninvasive positive pressure ventilation (Device)
Low-level ventilation
Each subject will receive 2 hours of low-level noninvasive positive pressure ventilation.
干预措施: noninvasive positive pressure ventilation (Device)
结局指标
主要结局
Difference in Pulmonary Function and Respiratory Muscle Pressure Testing
时间窗: 5 hours
Difference in Subjective Dyspnea Between Baseline and the Two Different Ventilator Modes
时间窗: 5 hours
Difference in Gas Exchange
时间窗: 5 hours
次要结局
未报告次要终点
研究者
Robert C. Basner
Special Lecturer in Medicine
Columbia University
