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Clinical Trial Summary

It is necessary for outcome measures to accurately reflect the state of health of a person in order for clinical trials to show benefit. The most commonly used outcome measure for Charcot Marie Tooth Disease (CMT) is the CMT Neuropathy Score, which uses cutoffs of points designated as mild (0-10 points), moderate (11-20) or severe (21-36). These terms are arbitrary. This study is looking to base mild, moderate, and severe on what both people affected with CMT and those who provide for people with CMT consider appropriate.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01455623
Study type Observational
Source University of Iowa
Contact
Status Completed
Phase N/A
Start date June 2011
Completion date March 2014

See also
  Status Clinical Trial Phase
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Completed NCT00541164 - Effects of Coenzyme Q10 on Charcot-Marie-Tooth Disease Phase 1/Phase 2
Recruiting NCT01918826 - Evaluation of the Analgesic Efficiency of the Transcutaneous Neurostimulation in the Charcot Syndrome Marie Tooth on the Pains of Lower Limbs N/A
Completed NCT02194010 - Disability Severity Scale (DSI) and Hereditary Motor and Sensory Neuropathy Overall Disability Scale (HMSN-R-ODS)
Recruiting NCT01203085 - Development of Charcot Marie Tooth Disease (CMT) Pediatric Scale for Children With CMT
Recruiting NCT01193075 - Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others