Effect of Noninvasive Ventilation on Lung Function in Amyotrophic Lateral Sclerosis

Columbia University

Status: Terminated

Conditions: Motor Neuron Disease; Amyotrophic Lateral Sclerosis

Treatments: Device: noninvasive positive pressure ventilation

Study type: Interventional

Funder types: Other

Identifiers

NCT00537446

AAAC7394

Details and patient eligibility

About

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.

Enrollment: 8 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

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8 participants in 2 patient groups

High-level ventilation

Active Comparator group

Description:

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

Treatment:

Device: noninvasive positive pressure ventilation

Device: noninvasive positive pressure ventilation

Low-level ventilation

Active Comparator group

Description:

Each subject will receive 2 hours of low-level noninvasive positive pressure ventilation.

Treatment:

Device: noninvasive positive pressure ventilation

Device: noninvasive positive pressure ventilation