Charcot-Marie-Tooth Disease Clinical Trials

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Investigation of Tremor in Patients With Charcot-Marie-Tooth Neuropathy

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Tremor is a symptom that has already been described in many case reports and case series concerning patients with Charcot-Marie-Tooth (CMT) disease. However, the pathophysiology of tremor in this condition remains largely unclear. It has also not been sufficiently investigated to what extent tremor in CMT patients constitutes a relevant impairment of quality of life. This project focuses on a more detailed characterization of tremor in CMT patients using surface electromyography and accelerometer analysis, as well as the collection of individual clinical data, particularly regarding the symptom of tremor, in order to facilitate the characterization and etiological classification of the tremor. In addition, a questionnaire-based assessment will be conducted to capture the impact of tremor on activities of daily living and the associated burden in this specific patient cohort. The entire data collection process will be supported by a clinical examination, which will be video-recorded by experienced neurologists to ensure more reliable analysis. This serves both the characterization of tremor and the illustration of its functional limitations. Where available, the data will be correlated with genetic variants to allow conclusions about possible genetic predispositions or disease progression. As a control group, CMT patients who have not yet reported a tremor will be included.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: t
View:

• Clinical CMT Diagnosis / Anamnestically Healthy Control Group

• Genetic confirmation of CMT in adult patients

• Ability to achieve the outcome measure at baseline

• Age between 18 and 65 years

• Capacity of all study participants to consent and signed informed consent, including patient or participant information and consent form

Locations
Other Locations
Germany
University Medical Centre
RECRUITING
Göttingen
Contact Information
Primary
Michael W Sereda, Prof. MD
sereda@mpinat.mpg.de
+49 551 3964162
Time Frame
Start Date: 2024-07-30
Estimated Completion Date: 2026-10-30
Participants
Target number of participants: 75
Treatments
CMT patients
Controls
Sponsors
Leads: University Medical Center Goettingen

This content was sourced from clinicaltrials.gov