Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
10000 participants
OBSERVATIONAL
2013-11-01
2029-12-31
Brief Summary
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Participants will be asked to complete a Natural History Survey.
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
All affected individuals with CMT/IN are eligible to participate in GRIN with proper informed consent.
Children, adolescents and adults with either a confirmed diagnosis or suspected to have CMT/IN are eligible with parent and/or guardian consent.
Individuals that have been clinically diagnosed through family history and/or standard clinical testing (e.g. neuro exam, EMG, NCS) and/or genetically tested or suspected to have CMT/IN (note: many mutations have not been identified yet) are eligible.
Exclusion Criteria
ALL
No
Sponsors
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Hereditary Neuropathy Foundation
OTHER_GOV
Responsible Party
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Principal Investigators
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Allison Moore
Role: PRINCIPAL_INVESTIGATOR
Hereditary Neuropathy Foundation
Locations
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Hereditary Neuropathy Foundation
New York, New York, United States
Countries
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Central Contacts
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Facility Contacts
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Related Links
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Landing page and entry for patients to participate in the Global Registry for Inherited Neuropathies
Other Identifiers
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GRIN1001
Identifier Type: -
Identifier Source: org_study_id
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