JPRN-UMIN000028736已完成未知
The randomized duble blind parallel-group comparison test of the effect for eye function of the Bilberry extract and Lutein - The randomized duble blind parallel-group comparison test of the effect for eye function of the Bilberry extract and Lutein
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 40
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 of serious diseases (e.g., cancer, cardiac arrest, cardiac infarct). 2, Subjects who have previous medical history and/or current medical history of serious diseases(e.g., arrhythmia, liver disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes, dyslipidemia, hypertension, other chronic diseases) 3, Subjects who have undergone gastrointestinal tract surgery; except appendectomy. 4, Subjects who take medicines. 5, Subjects who have an eye disease. 6, Subjects who are allergic to medicines or the test material of this trial. 7, Subjects who are or are possibly pregnant, or are lactating. 8, Subjects who participate in other clinical trials in the past 3 months. 9, Subjects who work time is irregular. 10, Smoker 11, Subjects who have been determined ineligible by principal 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 Bilberry extractseyestrainJPRN-UMIN000020866HUMA R&D Co.120
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
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
