Effect of Noninvasive Positive Pressure Ventilation on Pulmonary Function Testing in Amyotrophic Lateral Sclerosis
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Sponsor
- Columbia University
- Enrollment
- 8
- Locations
- 1
- Primary Endpoint
- Difference in Pulmonary Function and Respiratory Muscle Pressure Testing
Study Overview
Brief Summary
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Supportive Care
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 18 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •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
Exclusion Criteria
- •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.
Arms & Interventions
High-level ventilation
Each subject will spend 2 hours receiving high-level noninvasive ventilation.
Intervention: noninvasive positive pressure ventilation (Device)
Low-level ventilation
Each subject will receive 2 hours of low-level noninvasive positive pressure ventilation.
Intervention: noninvasive positive pressure ventilation (Device)
Outcomes
Primary Outcomes
Difference in Pulmonary Function and Respiratory Muscle Pressure Testing
Time Frame: 5 hours
Difference in Subjective Dyspnea Between Baseline and the Two Different Ventilator Modes
Time Frame: 5 hours
Difference in Gas Exchange
Time Frame: 5 hours
Secondary Outcomes
No secondary outcomes reported
Investigators
Robert C. Basner
Special Lecturer in Medicine
Columbia University
