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临床试验/NCT00683943
NCT00683943已完成1 期

Pilot Study of Tolerability of Lithium Therapy in Patients With Spinocerebellar Ataxia Type I (SCA1)

National Institute of Neurological Disorders and Stroke (NINDS)2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2008年5月18日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
13
试验地点
2
主要终点
Incidence of side effects, side effect profile, and number of falls.

研究概览

简要总结

This study will evaluate the side effects and tolerability of the drug lithium in patients with spinocerebellar ataxia type I (SCA1) an inherited disorder caused by loss of nerve cells in parts of the brain. Symptoms include ataxia (difficulty walking) and loss of muscle coordination and strength. Recent studies suggest that lithium may be helpful in treating some SCA1 symptoms.

People between 18 and 65 years of age with SCA1 who have only difficulty walking or who have difficulty walking as well as tremor, hand incoordination or speech problems, may be eligible for this study. Participation requires three hospital admissions at the NIH Clinical Center and one outpatient visit.

Participants undergo the following tests and procedures:

Admission 1 (2-6 weeks)

  • Medical history, physical examination, blood and urine tests, electrocardiogram.
  • Evaluation of SCA1 symptoms (balance, walking, dexterity, tremor, memory, mood and concentration).
  • Monitoring of liquid intake and output (urine) and weight changes.
  • Lithium treatment Start treatment and remain in hospital until the blood level of the drug is stabilized; continue treatment at home after hospital discharge.

Admission 2 (2-4 days, 4 weeks after hospital discharge).

  • Repeat of some or all of the procedures done at the first admission.
  • Continue lithium in hospital and at home after discharge, with local physician checking laboratory values as needed.

Admission 3 (2-4 days, 8 weeks after Admission 2).

  • Repeat of some or all of the procedures done at other admissions.
  • Stop lithium.

Outpatient Visit (4 weeks after Admission 3)

  • Evaluation of SCA1 symptoms.
  • Blood and urine tests.

详细描述

Objective

Evaluation of tolerability and safety of lithium in SCA1 patients.

Study Population

A total of 10 molecularly diagnosed SCA1 patients divided in two groups. One group would be composed of 5 patients with gait difficulty only and 5 patients with gait difficulty and tremor, hand incoordination or speech difficulties.

Design

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Incidence of side effects, side effect profile, and number of falls.

次要结局

  • ICARS scores, SARA scores, Quantitative Sway/Balance assessment, Tremor Rating Scale scores, dexterity evaluation, sleep questionnaire, Computerized Continuous Performing Tasks assessment

研究者

研究点 (2)

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