A Natural History Study of Charcot-Marie-Tooth

Brief Description Of Study

This is a longitudinal study of individuals with CMT looking at the natural history of the disease to see how it changes over time. Participants are invited back on a yearly basis to determine how the changes are occurring.

Clinical Study Identifier: TX1042

Detailed Study Description

The purpose of this research study is to develop a database to better understand Charcot-Marie-Tooth disease (CMT). We will carefully measure changes in strength, sensation, and nerve conduction velocities, using non-invasive but state of the art technology, at intervals of approximately six months to one year for as long as you would like to continue being seen at our practice. Individuals may also be eligible to enroll in our substudy, the Genetics of CMT. Genetic testing on a research basis is more thorough than commercial testing. People who are eligible include all people with CMT1A and families who have an unidentified form of CMT.

Additional Information About The Study

For more information, please reference the following links: https://www.rarediseasesnetwork.org/INC/studies/CMT-6601.htm and https://www.rarediseasesnetwork.org/INC/studies/CMT-6602.htm

Contact research investigator to learn more about this study by filling out the form below.

To: Research Study Investigator
Subject: I am interested in participating in your Research Study
Dear Investigator,
I'm interested in learning more about and participating in your research study named: A Natural History Study of Charcot-Marie-Tooth
I am hoping to hear back from you and discuss details of the study

By clicking "Contact Research Team", your contact information will be sent directly to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.