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Amyotrophic Lateral Sclerosis (ALS)NCT00420719

Motor-Point Stimulation for Conditioning the Diaphragm of Patients With Amyotrophic Lateral Sclerosis (ALS)

A study testing Intramuscular diaphragm electrodes in people with Amyotrophic Lateral Sclerosis (ALS), run by Synapse Biomedical at 8 sites in 2 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The overall goal of this research is to delay the respiratory decline of patients with Amyotrophic Lateral Sclerosis (ALS) thereby increasing their lifespan by conditioning the diaphragm with laparoscopically placed electrodes. This device currently holds an Investigational Device Exemption No. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Amyotrophic Lateral Sclerosis (ALS)
What is being tested?
Intramuscular diaphragm electrodes
How many people
100 participants
Where
8 sitesin 2 countries
Study dates
Oct 2004to Oct 2009
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age 18 or older
  • Participants with familial or sporadic ALS diagnosed as laboratory-supported probable, probable, or definite according to the World Federation of Neurology El Escorial criteria will be eligible
  • Bilateral phrenic nerve function clinically acceptable as demonstrated by bilateral diaphragm movement with fluoroscopic sniff test or with EMG recordings and nerve conduction times
  • Forced Vital Capacity (FVC) between 50 - 85% of predicted values to begin screening procedures.
  • FVC greater than 45% of predicted value at time of surgery.
  • No underlying cardiac or pulmonary diseases that would increase the risk of general anesthesia greater than the expected risk of the patient with ALS
  • Negative pregnancy test in females of child-bearing potential
  • Informed consent from patient or designated representative

Who cannot join

  • Preexisting implanted electrical device such as pacemaker or cardiac defibrillator.
  • Underlying pulmonary diseases that were present prior to ALS that would effect pulmonary tests independent of ALS
  • Active cardiovascular disease that would increase the risk of general anesthesia
  • Current pregnancy or breastfeeding
  • Hospitalization for a treated active infection within the last 2 months
  • Significant decision making incapacity preventing informed consent by the subject due to a major mental disorder such as major depression or schizophrenia, or dementia such as having Alzheimer's disease.
  • Marked obesity

Trial locations and contacts

8 sites in 2 countries.

8 sites in 2 countries

United States7 sites
  • Johns Hopkins University

    Baltimore, Maryland, 21287

  • University Hospitals Of Cleveland

    Cleveland, Ohio, 44106

  • Henry Ford Health System

    Detroit, Michigan, 48202-2689

  • The Methodist Hospital

    Houston, Texas, 77030

  • Mayo Clinic

    Jacksonville, Florida, 32224

  • Forbes Norris - California Pacific Medical Center (CPMC)

    San Francisco, California, 94115

  • Stanford University Medical Center

    Stanford, California, 94305

Other trials in United States

France1 site
  • Groupe Hospitalier Pitie-Salpetriere

    Paris

Other trials in France

About this study

Official title: Multi-Center Pivotal Study of Motor-Point Stimulation for Conditioning the Diaphragm of Patients With Amyotrophic Lateral Sclerosis (ALS)

The overall goal of this research is to delay the respiratory decline of patients with Amyotrophic Lateral Sclerosis (ALS) thereby increasing their lifespan by conditioning the diaphragm with laparoscopically placed electrodes.

This device currently holds an Investigational Device Exemption No. G040142 in the United States and is currently undergoing clinical trials at University Hospitals (Cleveland), Johns Hopkins, Mayo Clinic Jacksonville, California Pacific Medical Center (CPMC), Henry Ford Health System, The Methodist Hospital, and Stanford University.

Read the detailed description

The purpose of this study is to demonstrate the safety and efficacy of the NeuRX RA/4 Diaphragm Pacing Stimulation (DPS) System in conditioning the diaphragm of an ALS patient to improve the quality of life and slow the progression to respiratory failure.

Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's disease or Motor Neuron Disease) is a progressive neurodegenerative disease of unknown cause. One of the most important effects of progressive neuromuscular weakness in patients with ALS is the effect on respiration. Although ALS has no direct effect on the lung, it has devastating effects on mechanical function of the respiratory system. ALS affects all of the major respiratory muscle groups: upper airway muscles, expiratory muscles, and inspiratory muscles. Therefore, all patients with ALS are at significant risk for respiratory complications. Progressive inspiratory muscle weakness in ALS inevitably leads to carbon dioxide retention, inability to clear secretions and hypercarbic respiratory failure, the major cause of death in ALS.

Synapse Biomedical, in conjunction with Case Western Reserve University and University Hospitals of Cleveland, have evaluated activating the diaphragm with percutaneous intramuscular electrodes implanted laparoscopically. This eliminates any direct contact with the phrenic nerve, allows all circuitry and electronics to remain outside the body, and provides direct, selective activation to each hemidiaphragm. The NeuRx-RA/4 DPS System provides an electrical signal to the motor point of the muscle that causes the diaphragm to contract and allows patients to breathe more naturally.

The NeuRx RA/4 DPS System has been implanted in over 10 individuals with ALS, in a pilot study at the University Hospitals of Cleveland that began January, 2005.

The NeuRx RA/4 DPS System platform, also used for respiratory support for individuals with high-level spinal cord injury, has over 56 years of cumulative active implantation time. The longest term patient was implanted March 6, 2000 and has been using the DPS System as his sole means of respiratory support for over six years.

Given patient results to date the data supports safety and efficacy to proceed to pivotal study in this patient population. With no unexpected significant adverse events reported, the NeuRx RA/4 DPS System has performed reliably and safely.

Device Description: The NeuRx RA/4 Respiratory System is manufactured by Synapse Biomedical. The NeuRx RA/4 System comprises the following components: an external, battery powered Stimulator Device, an associated Programmer/Controller, Intramuscular Electrodes, associated percutaneous Lead Wires, a Surgical Placement Tool Set, and a surgical Mapping Station.

Inclusion Criteria:

  • Age 18 or older
  • Participants with familial or sporadic ALS diagnosed as laboratory-supported probable, probable, or definite according to the World Federation of Neurology El Escorial criteria will be eligible
  • Bilateral phrenic nerve function clinically acceptable as demonstrated by bilateral diaphragm movement with fluoroscopic sniff test or with EMG recordings and nerve conduction times
  • Forced Vital Capacity (FVC) between 50 - 85% of predicted values to begin screening procedures.
  • FVC greater than 45% of predicted value at time of surgery.
  • No underlying cardiac or pulmonary diseases that would increase the risk of general anesthesia greater than the expected risk of the patient with ALS
  • Negative pregnancy test in females of child-bearing potential
  • Informed consent from patient or designated representative

Exclusion Criteria:

  • Preexisting implanted electrical device such as pacemaker or cardiac defibrillator.
  • Underlying pulmonary diseases that were present prior to ALS that would effect pulmonary tests independent of ALS.
  • Active cardiovascular disease that would increase the risk of general anesthesia
  • Current pregnancy or breastfeeding
  • Hospitalization for a treated active infection within the last 2 months
  • Significant decision making incapacity preventing informed consent by the subject due to a major mental disorder such as major depression or schizophrenia, or dementia such as having Alzheimer's disease.
  • Marked obesity
Being tested
Intramuscular diaphragm electrodes
Keywords
ALS, Amyotrophic Lateral Sclerosis, Lou Gehrig's disease, Diaphragm for Ventilatory Assist, Diaphragm Pacing
Medical subject headings
Amyotrophic Lateral Sclerosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Intramuscular diaphragm electrodesDevice

    Conditioning of the diaphragm

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The DPS System will slow the decline of pulmonary function, as defined by percent predicted forced vital capacity (FVC) to 30% of normal, by approximately 12 months

    Measured: After completion of the study

Secondary outcomes (1)
  1. Adverse events from implantation and use of the DPS System will be logged and qualitatively compared to adverse event rates in similar patient populations.

    Measured: After completion of the study

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Jan 2007 (estimated)
  2. Study startOct 2004
  3. Primary completionOct 2009 (estimated)
  4. Study completionOct 2009 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00420719
Sponsor's protocol ID
CLIN 20-0009-0005
Status last verified
Mar 2009
First submitted
9 Jan 2007
Last updated
18 Mar 2009
Results posted
No

Publications

  • Gonzalez-Bermejo J, Morelot-Panzini C, Salachas F, Redolfi S, Straus C, Becquemin MH, Arnulf I, Pradat PF, Bruneteau G, Ignagni AR, Diop M, Onders R, Nelson T, Menegaux F, Meininger V, Similowski T. Diaphragm pacing improves sleep in patients with amyotrophic lateral sclerosis. Amyotroph Lateral Scler. 2012 Jan;13(1):44-54. doi: 10.3109/17482968.2011.597862. Epub 2011 Oct 24.

    PubMed 22023158

Questions about this trial

What is this clinical trial studying?

A study testing Intramuscular diaphragm electrodes in people with Amyotrophic Lateral Sclerosis (ALS), run by Synapse Biomedical at 8 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 18 Mar 2009. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 sites in United States, France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The DPS System will slow the decline of pulmonary function, as defined by percent predicted forced vital capacity (FVC) to 30% of normal, by approximately 12 months (time frame: After completion of the study). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00420719, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2009; AzTrials last refreshed its copy on 7 Nov 2026.

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