Full Text View
Tabular View
No Study Results Posted
Related Studies
Electrical Impedance Myography as an Outcome Measure in Amyotrophic Lateral Sclerosis Clinical Trials
This study is currently recruiting participants.
Study NCT00620698   Information provided by Beth Israel Deaconess Medical Center
First Received: February 9, 2008   Last Updated: August 28, 2009   History of Changes

February 9, 2008
August 28, 2009
May 2007
March 2009   (final data collection date for primary outcome measure)
 
 
Complete list of historical versions of study NCT00620698 on ClinicalTrials.gov Archive Site
 
 
 
Electrical Impedance Myography as an Outcome Measure in Amyotrophic Lateral Sclerosis Clinical Trials
Electrical Impedance Myography as an Outcome Measure in ALS Clinical Trials

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.

 
 
Observational
Cohort, Prospective
Amyotrophic Lateral Sclerosis
 
Patients with clinically established amyotrophic lateral sclerosis
Rutkove SB, Zhang H, Schoenfeld DA, Raynor EM, Shefner JM, Cudkowicz ME, Chin AB, Aaron R, Shiffman CA. Electrical impedance myography to assess outcome in amyotrophic lateral sclerosis clinical trials. Clin Neurophysiol. 2007 Nov;118(11):2413-8. Epub 2007 Sep 25.

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
120
December 2010
March 2009   (final data collection date for primary outcome measure)

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
Both
18 Years to 85 Years
No
Contact: Seward B. Rutkove, MD 617-667-8130 srutkove@bidmc.harvard.edu
United States
 
NCT00620698
Seward B. Rutkove, MD, Principal Investigator, Beth Israel Deaconess Medical Center
EIMALS
Beth Israel Deaconess Medical Center
ALS Association
Principal Investigator: Seward B Rutkove, MD Beth Israel Deaconess Medical Center
Principal Investigator: Jeremy M Shefner, MD, PhD Upstate Medical Center
Beth Israel Deaconess Medical Center
August 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP