Trial Search Results

Diaphragm Pacing System (DPS) In Participants With Amyotrophic Lateral Sclerosis (ALS)

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.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Barrow Neurological Institute

Collaborator: ALS Association

Stanford Investigator(s):


  • Device: NeuRx® Diaphragm Pacing System™ (DPS)


Phase 2


Inclusion Criteria:

   1. Age 21 years or older.

   2. Sporadic or familial ALS diagnosed as definite, probable or possible ALS as defined by
   revised El Escorial criteria.

   3. Evidence of hypoventilation at Screening with at least one of the following:

      1. Maximal static inspiratory pressure (MIP) <60 cm H20.

      2. Upright or supine forced vital capacity (FVC) <50% predicted for gender, age, and

   4. A phrenic nerve potential should be recordable bilaterally.

   5. 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).

   6. Capable of providing informed consent and following trial procedures.

   7. Geographically accessible to the site.

   8. 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).

   9. 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:

   1. Upright forced vital capacity (FVC) ≤ 45% of predicted for gender, age, and height.

   2. Any prior use of non-invasive ventilation (NIV) outside of sleep (nighttime or naps).

   3. Any pulmonary or cardiac disorder or other medical disorder that would be a
   contraindication for general anesthesia or DPS hardware implantation in the chest.

   4. Implanted electrical device such as a pacemaker or cardiac defibrillator.

   5. Known diaphragm abnormality such as hiatal hernia or para-esophageal hernia of
   abdominal contents into the thoracic cavity.

   6. Participation in another treatment research study for people with ALS.

   7. 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.

   8. Clinically significant history of unstable or severe cardiac, oncologic, hepatic,
   psychiatric, renal disease, or other medically significant illness.

   9. Pregnant women or women currently breastfeeding.

Ages Eligible for Study

21 Years - N/A

Genders Eligible for Study


Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Shirley Paulose
Not Recruiting