跳至主要内容
临床试验/NCT01057966
NCT01057966已完成4 期

Bioavailability of Nutrients Contained in Softgel Capsules vs Tablets

Alcon Research1 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1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
15
试验地点
1
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
是

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

研究组 & 干预措施

ICAPS AREDS Softgel Capsule - Full Strength

Experimental

ICAPS Eye Vitamin and Mineral Supplement - Softgel

干预措施: ICAPS Eye Vitamin and Mineral Supplement - Softgel (full strength) (Dietary Supplement)

ICAPS AREDS Softgel Capsule - Half Strength

Experimental

ICAPS Eye Vitamin and Mineral Supplement - Softgel (half -strength)

干预措施: ICAPS Eye Vitamin and Mineral Supplement - Softgel (half strength) (Dietary Supplement)

ICAPS AREDS coated tablets - Full Strength

Experimental

ICAPS Eye Vitamin and Mineral Supplement - Coated Tablets

干预措施: ICAPS Eye Vitamin and Mineral Supplement - Coated Tablets (full strength) (Dietary Supplement)

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 (1)

Loading locations...

相似试验