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临床试验/NCT00952393
NCT00952393已完成1 期

Nicotinic Receptors and Schizophrenia

VA Office of Research and Development1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
10
试验地点
1
主要终点
Blood Levels of Drug

研究概览

简要总结

The study determines if a new preparation of a drug designed to treat schizophrenia is more slowly released into the body.

详细描述

3-2,4 dimethoxybenzylidene will be compounded with a methyallose compound in doses of 150 and 300 mg. The capsules will be administered singly and eventually bid to determine if sustained blood levels comparable to steady state blood levels seen in previous studies can be determined. Safety and EEG effects will be measured.

研究设计

研究类型
Interventional
分配方式
Na
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

  • Healthy volunteers: males and females who are incapable of pregnancy

排除标准

  • Medical illnesses requiring acute treatment
  • History of seizures
  • Substance abuse including nicotine

研究组 & 干预措施

Pharmacokinetic

Other

This single arm examines the pharmaco-kinetics of the release of 3-2,4 dimethoxy-benzilidene anabaseine in a hypomellose sustained release formulation.

干预措施: Pharmacokinetic (Drug)

结局指标

主要结局

Blood Levels of Drug

时间窗: 12 hours

This is the plasma level of the drug as determined by high performance liquid chromatography.

次要结局

未报告次要终点

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (1)

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