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Follow up and Observation of Charcot Marie Tooth Disease in Families

This study has been completed.
Sponsor:
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT00149045
First received: September 7, 2005
Last updated: November 6, 2006
Last verified: August 2005
History of Changes
  Purpose

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


Condition
Charcot-Marie-Tooth Disease

Study Type: Observational
Study Design: Observational Model: Defined Population
Observational Model: Natural History
Time Perspective: Longitudinal
Time Perspective: Retrospective/Prospective
Official Title: Clinical and Genetic Features of Familial Neuropathy

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Hadassah Medical Organization:

Study Start Date: November 2001
Estimated Study Completion Date: August 2005
  Eligibility

Ages Eligible for Study:   8 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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

Exclusion Criteria:

-

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00149045

Locations
Israel
Hadassah Medical Organization
Jerusalem, Israel, 91120
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Israel Steiner, MD Hadssah University Hospital, Department of Neurology
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00149045     History of Changes
Other Study ID Numbers: 920010132-HMO-CTIL
Study First Received: September 7, 2005
Last Updated: November 6, 2006
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Hadassah Medical Organization:
familial peripheral Neuropathy Anticipation

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

ClinicalTrials.gov processed this record on June 17, 2013