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OpenTrials
Completed

NCT Number: NCT00537641

Efficacy of Noninvasive Ventilation in Amyotrophic Lateral Sclerosis (ALS)

This study will test the hypothesis that noninvasive ventilation (NIV) as prescribed in current medical practice for use in amyotrophic Lateral Sclerosis (ALS) patients fails to deliver adequate breathing support over a night of use in the patient's home. ALS patients who come to the ALS Center for their routine 3 month follow up exam and are currently using NIV will be asked to complete questionnaires regarding their quality of sleep, quality of life and general level of function, and to undergo a home sleep study, using a safe, comfortable and reliable breathing monitoring system during a night of sleep. If the questionnaires or the sleep study show failure of the breathing device, the investigators will work with the patient to fix the problem and then offer a second study to make sure that the changes were helpful. The results of this study may help to develop subsequent studies and to improve the guidelines used for care of ALS patients.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Eleanor and Lou Gehrig ALS/MDA Center at Columbia University

New York, 10032, United States

About this study

Amyotrophic Lateral Sclerosis (ALS), also known as "Lou Gehrig's Disease", is a fatal disorder that causes breathing failure due to progressive weakness of the muscles of breathing. Breathing assist devices known as noninvasive ventilation (NIV) are offered to ALS patients when their breathing function worsens. These devices deliver breathing assistance via a mask on the nose or nose and mouth, and are thought to be particularly important to be used during sleep, when breathing often becomes more shallow and irregular. However, although these devices have become the standard of therapy in ALS patients once their lung function worsens, it remains unclear how effective these devices actually are when a patient is sleeping, partly because of the practical difficulties in applying the device properly and keeping it applied throughout the sleep period, and partly because they are most commonly prescribed without objective evidence regarding how much breathing support the patient needs as the disease progresses and the breathing muscles weaken further.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • clinical diagnosis of amyotrophic lateral sclerosis (El Escorial criteria)
  • age 18 to 18 years old
  • using nocturnal noninvasive ventilation to treat respiratory insufficiency at least 4 hours per night, for at least 4 nights per week

Exclusion criteria

  • inability to safely use NIPPV because of bulbar dysfunction
  • indications for tracheostomy assisted ventilation due to inability to clear secretions from the airway
  • presence of comorbid conditions with a life expectancy < 6 months
  • presence of advanced dementia
  • unwillingness to follow up at the Eleanor and Lou Gehrig ALS/MDA Center at Columbia University on a regular basis
  • previously diagnosed obstructive sleep apnea
  • residence outside the New York metropolitan area.

Treatment and study plan

Primary outcomes

  1. Tolerance of bilevel PAP

    Time frame: Up to 3 months

    The ALS Functional Rating Scale - Revised (ALSFRS-R) will be administered to measure tolerance.

  2. Score on Epworth Sleepiness Scale

    Time frame: Up to 3 months

    Objective evidence of nocturnal sleep-disordered breathing on the bilevel PAP will be measured.

Sponsors and collaborators

Lead sponsor

Columbia University

Other

Registry information

Official study title

Prevalence and Severity of Nocturnal Oxygenation and Ventilation Failure in Patients With Amyotrophic Lateral Sclerosis Using Noninvasive Ventilation

Important dates

Study start
2007
Primary completion
2010
Study completion
2011
First posted
Oct 1, 2007
Registry last updated
Jul 7, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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