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临床试验/NCT01582113
NCT01582113已完成早期 1 期

Cognizin Citicoline Dosing in a Healthy Adolescent Male Population

Deborah Yurgelun-Todd1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2012年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
发起方
入组人数
84
试验地点
1
主要终点
Neurocognitive performance

研究概览

简要总结

To determine the functional effects of Citicoline, a natural supplement, when administered for a duration of four weeks (28 days) to non-psychiatric adolescent male participants. The investigators hypothesize that citicoline will provide cognitive benefits to this population after 28 days of supplementation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
13 Years 至 18 Years(Child, Adult)
性别
Male
接受健康志愿者

入选标准

  • Age 13-18 years old
  • No history of co-morbid psychiatric disorder, current Axis I or II diagnosis or previous pharmacotherapeutic trial

排除标准

  • Head injury with LOC > 5 minutes
  • Use of any psychotropic medication

研究组 & 干预措施

High Dose Citicoline

Experimental

At visit 1 and again at visit 2, participants assigned to the experimental arm will receive a 14-day supply of 500 mg of citicoline, of which they will be instructed to take 500 mg daily. This will be done in a double-blind, randomized fashion.

干预措施: Citicoline (Drug)

Low Dose Citicoline

Experimental

At visit 1 and again at visit 2, participants assigned to the experimental arm will receive a 14-day supply of 250 mg of citicoline, of which they will be instructed to take 250 mg daily. This will be done in a double-blind, randomized fashion.

干预措施: Citicoline (Drug)

Placebo

Placebo Comparator

At visit 1 and again at visit 2, participants assigned to the placebo group will be given 14-day supplies of placebo to be taken daily throughout the study period. This will be done in a double-blind, randomized fashion.

干预措施: Microcrystalline Cellulose (Other)

结局指标

主要结局

Neurocognitive performance

时间窗: 28 days

Using baseline assessment measures gathered at Visit 1, assessments collected at Visits 2 and 3 will be used to determine whether the combined administration of citicoline will improve neurocognitive performance in male adolescents.

次要结局

未报告次要终点

研究者

发起方
Deborah Yurgelun-Todd
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Deborah Yurgelun-Todd

Professor of Psychiatry

University of Utah

研究点 (1)

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