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Involvement of Lymphocyte Type B in Amyotrophic Lateral Sclerosis (ALS)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified February 2009 by Rambam Health Care Campus.
Recruitment status was:  Enrolling by invitation
Information provided by:
Rambam Health Care Campus Identifier:
First received: February 15, 2009
Last updated: February 17, 2009
Last verified: February 2009
The involvement of Lymphocyte type B in Amyotrophic lateral sclerosis (ALS) patients will be compared to lymphocyte in healthy subjects.

Amyotrophic Lateral Sclerosis

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Involvement of Lymphocyte Type B in Amyotrophic Lateral Sclerosis (ALS)

Resource links provided by NLM:

Further study details as provided by Rambam Health Care Campus:

Estimated Enrollment: 20
Study Start Date: August 2008
Estimated Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)
1 ALS patients
2 Healthy subjects


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Amyotrophic lateral sclerosis and Healthy subjects

Inclusion Criteria:

  • ALS patients who could sign ICF.

Exclusion Criteria:

  • No ALS patients age less than 18 years.
  Contacts and Locations
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Please refer to this study by its identifier: NCT00846560

Rambam Medical center, Neurology Department
Haifa, Israel
Sponsors and Collaborators
Rambam Health Care Campus
  More Information

Responsible Party: Prof. David Yarnitsky, Rambam medical center Identifier: NCT00846560     History of Changes
Other Study ID Numbers: ALS04CTIL
Study First Received: February 15, 2009
Last Updated: February 17, 2009

Additional relevant MeSH terms:
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Pathologic Processes
Neurodegenerative Diseases
Nervous System Diseases
Neuromuscular Diseases
Spinal Cord Diseases
Central Nervous System Diseases
TDP-43 Proteinopathies
Proteostasis Deficiencies
Metabolic Diseases processed this record on September 21, 2017