Noninvasive Ventilation in ALS Patients With Mild Respiratory Involvement

Johns Hopkins University

Status and phase

Completed

Phase 3

Phase 2

Conditions

Amyotrophic Lateral Sclerosis

Treatments

Device: noninvasive positive pressure ventilation

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT00386464

HL 67887-03

Details and patient eligibility

About

Non-invasive ventilation or BiPAP®, which is a form of breathing support delivered through a facemask, is a successful treatment for the respiratory complications of amyotrophic lateral sclerosis (ALS). It has been shown to prolong survival, improve quality of life, and improve cognitive function. It is widely used among patients with ALS who have advanced breathing difficulties. It is not known whether there is benefit to using non-invasive ventilation earlier in the disease course.

There is evidence that non-invasive ventilation may slow down the decline in breathing function. If this were true then it would make sense to start non-invasive ventilation use earlier than the current clinically accepted practices.

The purpose of this study is to determine whether using non-invasive ventilation early in the course of disease can slow the decline in breathing function.

Patients remain in the study for 6 months and are asked to make 7 clinic visits during which time they will undergo pulmonary function tests and complete questionnaires.

Full description

This is a randomized, crossover trial for patient with ALS and mild respiratory involvement. Patients with forced vital capacity above 60% of the predicted value can join. Patients will be assigned to either start using non-invasive ventilation at night or continue their usual care. After three months, patients will switch over to the other treatment group. For example, a patient who was initially assigned to continue their usual care would begin using non-invasive ventilation after three months.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Probable or definite ALS by El Escorial criteria
age >17 years
FVC >60
minimal respiratory symptoms (no orthopnea or dyspnea at rest)
ability to provide informed consent

Exclusion criteria

Presence of another neurodegenerative disease
arterial CO2 above 45 mmHg
O2 below 60 mmHg
coexisting chronic lung disease unrelated to ALS
presence of an unstable medical condition such as coronary artery disease, liver failure, renal failure or cancer in the 30 days preceding enrollment