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临床试验/NCT01057966
NCT01057966已完成4 期

Bioavailability of Nutrients Contained in Softgel Capsules vs Tablets

Alcon Research2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2010年2月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
15
试验地点
2
主要终点
Bioavailability of nutrients

研究概览

简要总结

This study is a comparison of the bioavailability of nutrients contained in softgel capsules vs tablets.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 to 35
  • Body Mass Index (BMI) 21-27 kg/m2
  • Must be able to give written informed consent
  • Subjects must be willing to comply with all study requirements.
  • Subjects must understand, sign and be given a copy of the written Informed Consent form.

排除标准

  • Subjects for whom both eyes do not meet all inclusion criteria and either eye meets exclusion criteria
  • Subjects who are pregnant, lactating or planning to be pregnant during the course of the study
  • Subjects with known sensitivity to planned study concomitant medications
  • Subjects participating in any other ophthalmic drug or device clinical trial within 30 days of this clinical investigation.
  • Use of ocular drugs, other than study medications, during the study and within 14 days prior to study entry or any other ocular medication

结局指标

主要结局

Bioavailability of nutrients

时间窗: 1 week for each treatment cross-over period

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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