Recruiting NCT04010188
A Registered Cohort Study on Charcot-Marie-Tooth Disease
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Charcot-Marie-Tooth Disease. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Registered Observational Cohort Study of Charcot-Marie-Tooth Disease
Overview
The aim of the study is to analyze the natural history data data from Charcot-Marie-Tooth disease and related disorders in China, to assess the clinical, genetic, epigenetic features of patients with Charcot-Marie-Tooth disease, and to optimize clinical management.
Primary outcome measures
- The change of Charcot-Marie-Tooth Neuropathy Score (CMTNS) during 6 month [Time frame: Up to 6 months]
Eligibility criteria
Inclusion criteria
- Patients with the clinical diagnosis of Charcot-Marie-Tooth disease
- Genetic diagnosis of patients with Charcot-Marie-Tooth disease
- Unrelated healthy controls
Exclusion criteria
- Decline to participate.
- Other peripheral neuropathy caused by trauma, immunity and toxicosis.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- First Affiliated Hospital of Fujian Medical University — Fuzhou
Identifiers
NCT: NCT04010188 · MRCTA,ECFAH of FMU [2019] 192