JPRN-UMIN000020866已完成未知
The randomized duble blind parallel-group comparison test of the effect for eyestrain of the Bilberry extracts - The test of the effect for eyestrain of the Bilberry extracts
HUMA R&D Co.0 个研究点目标入组 120 人开始时间: 2016年2月3日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 60years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •1, Subjects who have previous medical history and/or current medical history of serious diseases (e.g., digestive organ, liver, pancreas, heart and/or kidney). 2, Subjects who take medicines. 3, Subjects who have an eye disease. 4, Subjects who have previous medical history of drug and/or food allergy. 5, Subjects who have previous medical history and/or current medical history of drug dependence and/or drug abuse. 6, Subjects who work time is irregular. 7, Subjects who have undergone LASIK. 8, Subjects who are using the reading glasses. 9, Subjects who constantly use supplements containing bilberry extract and/or functional foods or drug affecting eyestrain. 10, Subjects who have been enrolled in the other clinical trials within about last 1 month. 11, Subjects who is during pregnancy, lactation and/or wish to become pregnant in clinical test. 12, Subjects who have taken over 200 mL of blood within the last one month prior to the current study. 13, Subjects who have been determined ineligible by principal investigator or sub-investigator.
研究者
相似试验
已完成
不适用
The randomized duble blind parallel-group comparison test of the effect for eyestrain of the functional food including Bilberry extractsJPRN-UMIN000015253Department of Ophthalmology , Health Sciences University of Hokkaido Hospital30
已完成
不适用
The randomized duble blind parallel-group comparison test of the effect for eye function of the Bilberry extract and Luteihealthy subjectJPRN-UMIN000028736Omnica Co.,Ltd40
已完成
4 期
A clinical study to evaluate efficacy and safety of inhaled corticosteroids in mild to moderate cases of Chronic Obstructive Pulmonary DiseaseCTRI/2011/091/000182Research project grant of Government of Gujarat60
进行中(未招募)
不适用
A Randomized, Double Blind, Parallel-Group Comparative Study of Flexibly Dosed Paliperidone Palmitate(25, 50, 75, 100 mg eq) Administered Every 4 Weeks and Flexibly Dosed Risperdal Consta (25, 37.5, or 50 mg) Administered Every 2 Weeks in Subjects with Schizophrenia - ComparativeschizophreniaEUCTR2004-002694-22-EEJanssen-Cilag International NV700
已完成
不适用
Randomized, double-blind, parallel group comparison trial of Tocilizumab for colchicine-resistant familial Mediterranean feverfamilial Mediterranean feverJPRN-UMIN000028010Department of Immunology and Rheumatology, Division of Advanced Preventive Medical Sciences, Nagasaki University Graduate School of Biomedical Sciences23
