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临床试验/NCT01468948
NCT01468948已完成1 期

Dose Escalation Study of Oral Octanoic Acid in Patients With Essential Tremor

National Institute of Neurological Disorders and Stroke (NINDS)2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2011年10月28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
18
试验地点
2
主要终点
Dose-limiting toxicity

研究概览

简要总结

Background:

  • Essential tremor (ET) is a condition of out-of-control shaking. Several drugs are used to treat ET. However, they are often only partly helpful and can have side effects. Many people with ET get some relief from drinking alcohol. Octanol, a food additive similar to alcohol, can improve tremor in animals and is less likely to make people feel drunk. One form of octanol, called 1-octanol, has been shown to improve tremor in some people and had few side effects. 1-octanol is converted to octanoic acid, and research suggests that octanoic acid itself might suppress ET with no significant side effects such as drunkenness. Researchers want to see what dose of octanoic acid is most useful in reducing ET.

Objectives:

  • To test different doses of octanoic acid to treat essential tremor.

Eligibility:

  • Individuals at least 21 years of age who have ET that responds to treatment with alcohol.
  • Participants must be able to stop taking certain ET medications during the study.

Design:

  • This study requires three visits. Visit 1 is a screening visit that will take up to 5 hours. Visit 2 is a 2- to 3-day inpatient admission to the National Institutes of Health Clinical Center. Visit 3 is a followup outpatient visit 1 to 2 weeks after the hospital admission.
  • At the screening visit, participants will have a physical exam, neurological exam, and medical history. Blood and urine samples will be collected. Participants will also have an alcohol dose test to measure the tremor s response to alcohol.
  • For the study visit, participants will enter the hospital for testing. Participants will have the study drug and test the tremor's response to it. Frequent blood samples will be collected.
  • One to two weeks after leaving the hospital, participants will have a final followup study visit. Blood samples will be collected.

详细描述

OBJECTIVE:

To determine the maximum tolerated dose of oral octanoic acid (OA) in patients with essential tremor. Further study objectives include the evaluation of the efficacy and tolerability of octanoic acid with escalation doses, as well as the pharmacokinetic and pharmacodynamic profile.

STUDY POPULATION:

Up to 30 subjects with ethanol-responsive essential tremor (ET) will be included in the study. Subjects will be recruited in groups of 6 per dose level.

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
21 Years 至 —(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

Dose-limiting toxicity

时间窗: 2 years

次要结局

  • Effect on tremor(2 years)

研究者

研究点 (2)

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Octanoic Acid for Essential Tremor | 临床试验