N/A
N=89
Electrical Impedance Myography as an Outcome Measure in Amyotrophic Lateral Sclerosis Clinical Trials
Amyotrophic Lateral Sclerosis
Bottom Line
View on ClinicalTrials.gov: NCT00620698 ↗Enrolled (actual)
89
Serious AEs
0.0%
Results posted
Sep 2014
Primary outcome: Primary: Electrical Impedance Myography — 0.55 Coefficient of Variation
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Beth Israel Deaconess Medical Center
- Primary completion
- Mar 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Electrical Impedance Myography |
0.55 | — |
| SECONDARY ALS Functional Rating Scale |
0.84 | — |
| SECONDARY Handheld Dynamometry |
0.925 | — |
Summary
Trials evaluating new therapies for stopping or slowing the progression of ALS depend critically upon the use of outcome measures to assess whether a potential treatment is effective. The more effective an outcome measure, the fewer patients need to be enrolled and the shorter the trial. Many outcome measures have been used over the years, including strength assessments, breathing tests, functional status surveys, and nerve testing, but all are far from ideal. A new method, called electrical impedance myography (EIM) appears to be especially promising in that it provides very consistent data from one testing session to the next, is sensitive to the muscle deterioration that occurs in ALS, and is entirely painless and non-invasive. In this study, investigators from multiple institutions plan to compare several different outcome measures, including EIM, in approximately 120 ALS patients, with each patient being followed for a period of one year. All of these measures will be compared to one another and an assessment of their ability to detect disease progression made. Our goal will be to determine whether EIM can serve as a valuable new outcome measure, ultimately leading to substantially faster, more effective ALS trials requiring fewer patients.
Eligibility Criteria
Inclusion Criteria
- Definite or probably ALS by El Escorial criteria
- Muscle strength of at 3.5 in one limb
Exclusion Criteria
- Forced vital capacity of less than 70%
- Atypical forms of motor neuron disease (monomelic amyotrophy, primary lateral sclerosis)
- Pacemaker
Data sourced from ClinicalTrials.gov (NCT00620698). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.