Noninvasive Ventilation in ALS Patients With Mild Respiratory Involvement

NCT ID: NCT00386464

Last Updated: 2007-11-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-04-30
• Study Completion Date: 2007-09-30

Brief Summary

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.

Detailed 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.

Conditions

Amyotrophic Lateral Sclerosis

Keywords

bipap; lou gehrigs disease; motor neuron disease; respiratory muscles

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Interventions

noninvasive positive pressure ventilation

Intervention Type: DEVICE

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)

NIH

Sponsor Role: collaborator

Johns Hopkins University

OTHER

Sponsor Role: lead

Principal Investigators

Noah Lechtzin, MD

Role: PRINCIPAL_INVESTIGATOR

Johns Hopkins University

Charles M Wiener, MD

Role: STUDY_CHAIR

Johns Hopkins University

Locations

Johns Hopkins University School of Medicine

Baltimore, Maryland, United States

Countries

United States

Related Links

http://www.hopkinsneuro.org/ALS/clinical_trials.cfm

Johns Hopkins ALS Center

Other Identifiers

HL 67887-03

Identifier Type: -

Identifier Source: org_study_id