Follow up and Observation of Charcot Marie Tooth Disease in Families

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00149045
Recruitment Status : Completed
First Posted : September 8, 2005
Last Update Posted : November 7, 2006
Information provided by:
Hadassah Medical Organization

Brief Summary:
The study is aimed to test the hypothesis that there is anticipation in CMT

Condition or disease
Charcot-Marie-Tooth Disease

Study Type : Observational
Observational Model: Defined Population
Observational Model: Natural History
Time Perspective: Longitudinal
Time Perspective: Retrospective/Prospective
Official Title: Clinical and Genetic Features of Familial Neuropathy
Study Start Date : November 2001
Estimated Study Completion Date : August 2005

Information from the National Library of Medicine

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Ages Eligible for Study:   8 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:Patients with Genetically confirmed CMT 1a disease -

Exclusion Criteria:

Information from the National Library of Medicine

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 identifier (NCT number): NCT00149045

Hadassah Medical Organization
Jerusalem, Israel, 91120
Sponsors and Collaborators
Hadassah Medical Organization
Principal Investigator: Israel Steiner, MD Hadssah University Hospital, Department of Neurology Identifier: NCT00149045     History of Changes
Other Study ID Numbers: 920010132-HMO-CTIL
First Posted: September 8, 2005    Key Record Dates
Last Update Posted: November 7, 2006
Last Verified: August 2005

Keywords provided by Hadassah Medical Organization:
familial peripheral Neuropathy Anticipation

Additional relevant MeSH terms:
Tooth Diseases
Charcot-Marie-Tooth Disease
Nerve Compression Syndromes
Hereditary Sensory and Motor Neuropathy
Stomatognathic Diseases
Nervous System Diseases
Heredodegenerative Disorders, Nervous System
Neurodegenerative Diseases
Peripheral Nervous System Diseases
Neuromuscular Diseases
Genetic Diseases, Inborn
Nervous System Malformations
Congenital Abnormalities