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临床试验/NCT07570459
NCT07570459招募中不适用

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

University Medical Center Goettingen1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2024年7月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
75
试验地点
1
主要终点
Activities of Daily Living -Questionaire(ADL)

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • Pregnancy or breastfeeding period
  • Other relevant neurological or psychiatric disorders, acute or in the past history
  • Presence of a serious previous internal disease

研究组 & 干预措施

CMT patients

Controls

结局指标

主要结局

Activities of Daily Living -Questionaire(ADL)

时间窗: baseline

Assessment of Handicap - Questionaire

时间窗: baseline

Fahn Tolosa Marin Rating Scale

时间窗: baseline

Electrophysiological characterization of tremor using surface EMG and accelerometer analysis

时间窗: baseline

次要结局

  • MDS-UPDRS Part III without Tremor(baseline)
  • SARA Score(baseline)

研究者

发起方
University Medical Center Goettingen
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael W Sereda, MD, Professor of Neurology

Prof. Michael Sereda MD

University Medical Center Goettingen

研究点 (1)

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