Electrical Impedance Myography as an Outcome Measure in Amyotrophic Lateral Sclerosis Clinical Trials
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ClinicalTrials.gov Identifier: NCT00620698 |
Recruitment Status :
Completed
First Posted : February 21, 2008
Results First Posted : September 10, 2014
Last Update Posted : September 25, 2014
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Condition or disease |
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Amyotrophic Lateral Sclerosis |
Study Type : | Observational |
Actual Enrollment : | 89 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Official Title: | Electrical Impedance Myography as an Outcome Measure in ALS Clinical Trials |
Study Start Date : | May 2007 |
Actual Primary Completion Date : | March 2011 |
Actual Study Completion Date : | March 2012 |

Group/Cohort |
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ALS patients
Patients with clinically established amyotrophic lateral sclerosis
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- Electrical Impedance Myography [ Time Frame: 6 months ]The main outcome measure was the coefficient of variation (CoV) in the rate of the decline for each measure over time. The CoV was calculated by dividing the standard deviation in the rate of decline across the group of subjects and dividing that by the mean rate of decline for the cohort. This approach was taken for each of the measures being evaluated (ALS Functional Rating Scale-Revised, Handheld dynamometry, Electrical impedance myography). The lower the CoV in the rate of decline, the more sensitive it is to identifying a potential treatment effect, since it suggests gives a measure of homogeneity of the rate of decline across the population as well as the overall rate of decline. The smaller the standard deviation across the group and the larger the mean rate of decline across the group, the lower the CoV and the fewer number of subjects needed for a potential clinical trial using that outcome measure.
- ALS Functional Rating Scale [ Time Frame: 6 months ]The main outcome measure was the coefficient of variation (CoV) in the rate of the decline for each measure over time. The CoV was calculated by dividing the standard deviation in the rate of decline across the group of subjects and dividing that by the mean rate of decline for the cohort. This approach was taken for each of the measures being evaluated (ALS Functional Rating Scale-Revised, Handheld dynamometry, Electrical impedance myography). The lower the CoV in the rate of decline, the more sensitive it is to identifying a potential treatment effect, since it suggests gives a measure of homogeneity of the rate of decline across the population as well as the overall rate of decline. The smaller the standard deviation across the group and the larger the mean rate of decline across the group, the lower the CoV and the fewer number of subjects needed for a potential clinical trial using that outcome measure.
- Handheld Dynamometry [ Time Frame: 6 months ]The main outcome measure was the coefficient of variation (CoV) in the rate of the decline for each measure over time. The CoV was calculated by dividing the standard deviation in the rate of decline across the group of subjects and dividing that by the mean rate of decline for the cohort. This approach was taken for each of the measures being evaluated (ALS Functional Rating Scale-Revised, Handheld dynamometry, Electrical impedance myography). The lower the CoV in the rate of decline, the more sensitive it is to identifying a potential treatment effect, since it suggests gives a measure of homogeneity of the rate of decline across the population as well as the overall rate of decline. The smaller the standard deviation across the group and the larger the mean rate of decline across the group, the lower the CoV and the fewer number of subjects needed for a potential clinical trial using that outcome measure.

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Ages Eligible for Study: | 18 Years to 85 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00620698
United States, Florida | |
University of Miami Miller School of Medicine | |
Miami, Florida, United States, 33136 | |
United States, Georgia | |
Emory University | |
Atlanta, Georgia, United States | |
United States, Maryland | |
Johns Hopkins | |
Baltimore, Maryland, United States | |
United States, Massachusetts | |
Beth Israel Deaconess Medical Center | |
Boston, Massachusetts, United States, 02446 | |
Massachusetts General Hospital | |
Boston, Massachusetts, United States | |
United States, New York | |
Upstate Medical Center | |
Syracuse, New York, United States | |
United States, North Carolina | |
Wake Forest University Baptist Medical Center | |
Winston-Salem, North Carolina, United States, 27157 | |
United States, Virginia | |
University of Virginia Medical Center | |
Charlottesville, Virginia, United States, 22908 |
Principal Investigator: | Seward B Rutkove, MD | Beth Israel Deaconess Medical Center | |
Principal Investigator: | Jeremy M Shefner, MD, PhD | Upstate Medical Center |
Responsible Party: | Seward Rutkove, Principal Invesigator, Beth Israel Deaconess Medical Center |
ClinicalTrials.gov Identifier: | NCT00620698 |
Other Study ID Numbers: |
EIMALS |
First Posted: | February 21, 2008 Key Record Dates |
Results First Posted: | September 10, 2014 |
Last Update Posted: | September 25, 2014 |
Last Verified: | September 2014 |
amyotrophic lateral sclerosis motor neuron disease outcome measure biomarker impedance |
Motor Neuron Disease Amyotrophic Lateral Sclerosis Sclerosis Pathologic Processes Neurodegenerative Diseases Nervous System Diseases |
Neuromuscular Diseases Spinal Cord Diseases Central Nervous System Diseases TDP-43 Proteinopathies Proteostasis Deficiencies Metabolic Diseases |