A study examining the effects of continuous intake of test food on eye function and QO
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000035171
- Lead Sponsor
- IMEQRD Co., Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 58
Not provided
1.Those who currently receive some types of drug treatment (except for the drugs that are taken as needed) 2.Those who currently undergo dietary or exercise therapy under the supervision of a physician 3.Those with a history of treatment for malignant tumor, heart failure, or heart attack 4.Those who have undergone gastrointestinal surgery (except for appendectomy) 5.Those with a past medical history of any of the following: hepatic or other major disorders (kidneys, endocrine, cardiovascular, gastrointestine, lungs, blood, and metabolism), or complications of the disorders listed above 6.Those who have undergone laser-assisted in-situ keratomileusis in the past six months 7.Those with eye diseases, except for ametropia (hyperopia, myopia, and astigmatism) 8.Those who currently take health food (such as food products to maintain or restore health and supplements) 9.Those with a past and current medical history of drug or food allergy 10.Those who work irregularly, such as night shifts and irregular shifts 11.Those who have participated in another clinical trial within a month prior to submission of an informed consent document 12.Those who are currently pregnant or breastfeeding and those who desire a pregnancy 13.In the opinion of the principal investigator, those who were determined to be unsuitable for participation in this clinical trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method