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临床试验/NCT00537446
NCT00537446终止不适用

Effect of Noninvasive Positive Pressure Ventilation on Pulmonary Function Testing in Amyotrophic Lateral Sclerosis

Columbia University1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2007年9月1日最近更新:
适应症
干预措施

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

Active Comparator

Each subject will spend 2 hours receiving high-level noninvasive ventilation.

干预措施: noninvasive positive pressure ventilation (Device)

Low-level ventilation

Active Comparator

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

申办方类型
Other
责任方
Principal Investigator
主要研究者

Robert C. Basner

Special Lecturer in Medicine

Columbia University

研究点 (1)

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