跳至主要内容
临床试验/NL-OMON31178
NL-OMON31178已完成不适用

Track-HD - Track-HD

eids Universitair Medisch Centrum0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational invasive

入排标准

年龄范围
18 至 99(—)

入选标准

  • Ability to tolerate MRI and sample donation;• Subjects will be either:
  • 1. Control subject
  • a. Partner/spouse of a patient, not at risk of HD
  • b. Known non-carriers for HD (after genetic testing);2. Premanifest gene carrier
  • a. Positive genetic test with CAG repeat length >= 40 and
  • b. Burden of pathology score [(CAG-35.5) × age] >250 and
  • c. Absence of diagnostic motor features according to the UHDRS 99;3. Early HD
  • a. Positive genetic test with CAG repeat length >= 40 and
  • b. Presence of diagnostic motor features according to the UHDRS 99 and
  • c. Shoulson and Fahn stage 1 (TFC > 9-13) or 2 (TFC >= 7) according to the UHDRS 99 - functional capacity

排除标准

  • Stage 3 (TFC <= 6) or greater at time of enrolment
  • Less than 18 years of age
  • More than 65 years of age
  • Major psychiatric disorder at time of enrolment
  • Concomitant significant neurological disorder
  • Concomitant significant medical illness
  • Unsuitability for MRI, e.g. claustrophobia, metal implants
  • Unwillingness to donate blood
  • History of significant head injury
  • Drug and/or alcohol abuse
  • Significant hand injuries that preclude either writing or rapid computerized responding
  • Currently participating in a clinical drug trial

研究者

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