Multiple Sclerosis Clinical Trial
Diaphragm Pacing System (DPS) In Participants With Amyotrophic Lateral Sclerosis (ALS)
Summary
The study is being conducted to determine if DPS treatment for people with ALS and hypoventilation is associated with improved survival or diaphragm function.
The primary objective of the study is to conduct a multi-center, randomized controlled clinical trial comparing standard of care (control) to diaphragm stimulator treatment with the NeuRx® Diaphragm Pacing System™ (DPS) with respect to survival.
The secondary objective of the study is to conduct a multi-center, randomized controlled clinical trial to compare standard of care treatment (control) to DPS in ALS subjects with hypoventilation.
Full Description
The study is a randomized controlled study to compare standard of care (control) to DPS (diaphragm stimulator named The NeuRx® Diaphragm Pacing System™). Although it remains uncertain if DPS is efficacious for the ALS subject, given the preliminary studies performed by the device manufacturer, it has received FDA humanitarian device exemption (HDE) approval as a humanitarian use device (HUD). This study will utilize a 2:1 randomization schedule such that eligible ALS subjects will have a 2/3 chance of receiving DPS and 1/3 chance of standard of care (control) treatment.
The NeuRx® Diaphragm Pacing System™ (DPS) is a four channel, implanted percutaneous diaphragm muscle stimulation system. Under general anesthesia, the intramuscular electrodes are laparoscopically implanted in the diaphragm. The ends of the implanted electrodes are tunneled subcutaneously to an exit site on the chest or abdominal wall and connected to an external stimulator.
Eligibility Criteria
Inclusion Criteria:
Age 21 years or older.
Sporadic or familial ALS diagnosed as definite, probable or possible ALS as defined by revised El Escorial criteria.
Evidence of hypoventilation at Screening with at least one of the following:
Maximal static inspiratory pressure (MIP) <60 cm H20.
Upright or supine forced vital capacity (FVC) <50% predicted for gender, age, and height.
A phrenic nerve potential should be recordable bilaterally.
Subjects must not have taken riluzole for at least 30 days, or be on a stable dose of riluzole for at least 30 days, prior to randomization (riluzole-naïve subjects are permitted in the study).
Capable of providing informed consent and following trial procedures.
Geographically accessible to the site.
Negative urine pregnancy test at Screening in women of child bearing potential (WOCBP). (Women who are post-menopausal or who have had a hysterectomy are deemed not of child bearing potential).
Women of child bearing potential must use an adequate form of contraception: abstinence, hormonal contraception (oral contraception, implanted contraception, injected contraception or other hormonal (patch or contraceptive ring, for example) contraception), intrauterine device (IUD) in place for ≥ 3 months, barrier method in conjunction with spermicide, or another adequate method.
Exclusion Criteria:
Upright forced vital capacity (FVC) ≤ 45% of predicted for gender, age, and height.
Any prior use of non-invasive ventilation (NIV) outside of sleep (nighttime or naps).
Any pulmonary or cardiac disorder or other medical disorder that would be a contraindication for general anesthesia or DPS hardware implantation in the chest.
Implanted electrical device such as a pacemaker or cardiac defibrillator.
Known diaphragm abnormality such as hiatal hernia or para-esophageal hernia of abdominal contents into the thoracic cavity.
Participation in another treatment research study for people with ALS.
Exposure to any other agent currently under investigation for the treatment of people with ALS (off-label use or investigational) within 30 days of the Screening Visit.
Clinically significant history of unstable or severe cardiac, oncologic, hepatic, psychiatric, renal disease, or other medically significant illness.
Pregnant women or women currently breastfeeding.
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
Phoenix Arizona, , United States
Los Angeles California, , United States
San Diego California, , United States
Stanford California, , United States
New Britain Connecticut, , United States
Jacksonville Florida, , United States
Jacksonville Florida, , United States
Iowa City Iowa, , United States
Boston Massachusetts, , United States
Detroit Michigan, , United States
Saint Louis Missouri, , United States
Lincoln Nebraska, , United States
New York New York, , United States
Syracuse New York, , United States
Charlotte North Carolina, , United States
Winston-Salem North Carolina, , United States
Cleveland Ohio, , United States
Columbus Ohio, , United States
Portland Oregon, , United States
Philadelphia Pennsylvania, , United States
Pittsburgh Pennsylvania, , United States
Dallas Texas, , United States
San Antonio Texas, , United States
Burlington Vermont, , United States
Seattle Washington, , United States
How clear is this clinincal trial information?