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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.
 
ClinicalTrials.gov Identifier: NCT00149045
Recruitment Status : Completed
First Posted : September 8, 2005
Last Update Posted : November 7, 2006
Sponsor:
Information provided by:
Hadassah Medical Organization

Tracking Information
First Submitted Date September 7, 2005
First Posted Date September 8, 2005
Last Update Posted Date November 7, 2006
Study Start Date November 2001
Primary Completion Date Not Provided
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History Complete list of historical versions of study NCT00149045 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Follow up and Observation of Charcot Marie Tooth Disease in Families
Official Title Clinical and Genetic Features of Familial Neuropathy
Brief Summary The study is aimed to test the hypothesis that there is anticipation in CMT
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Defined Population
Observational Model: Natural History
Time Perspective: Longitudinal
Time Perspective: Retrospective/Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Not Provided
Study Population Not Provided
Condition Charcot-Marie-Tooth Disease
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Enrollment Not Provided
Original Enrollment Not Provided
Study Completion Date August 2005
Primary Completion Date Not Provided
Eligibility Criteria

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

Exclusion Criteria:

-

Sex/Gender
Sexes Eligible for Study: All
Ages 8 Years and older   (Child, Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Israel
Removed Location Countries  
 
Administrative Information
NCT Number NCT00149045
Other Study ID Numbers 920010132-HMO-CTIL
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Not Provided
Study Sponsor Hadassah Medical Organization
Collaborators Not Provided
Investigators
Principal Investigator: Israel Steiner, MD Hadssah University Hospital, Department of Neurology
PRS Account Hadassah Medical Organization
Verification Date August 2005