Unique ID issued by UMIN | UMIN000000635 |
---|---|
Receipt number | R000000769 |
Scientific Title | Efficacy of lutein supplement on macular pigments density and visual performance of age-related macular degeneration (AMD) patients |
Date of disclosure of the study information | 2007/03/11 |
Last modified on | 2009/09/11 16:14:54 |
Efficacy of lutein supplement on macular pigments density and visual performance of age-related macular degeneration (AMD) patients
Efficacy of lutein supplement on age-related macular degeneration
Efficacy of lutein supplement on macular pigments density and visual performance of age-related macular degeneration (AMD) patients
Efficacy of lutein supplement on age-related macular degeneration
Japan |
age-related macular degeneration (AMD) patients
Ophthalmology |
Others
NO
We will measure the macular pigment density and the change of visual functions after administration of lutein supplements on age-related macular degeneration patients, and evaluate the therapeutic effects of lutein for age-related macular degeneration.
Efficacy
Not applicable
Measurements of visual acuity, contrast sensitivity, metamorphopsia graded by M-chart, perimetric mean sensitivity, and macular pigment density
Interventional
Parallel
Randomized
Double blind -all involved are blinded
Placebo
2
Treatment
Food |
One capsule containing 10 mg of lutein and 0.8 mg of zeaxanthin is administered to each participants once a day for 12 months
One capsule of placebo supplement is administered to each participants once a day for 12 months
50 | years-old | <= |
Not applicable |
Male and Female
(1) Patients having either early age-related maculopathy (ARM), exudative age-related macular degeneration (AMD), or atrophic AMD
(2) Patients showing either visual acuity of less than 1.0, decreased contrast sensitivity, metamorphopsia detected by M-cahrt, or decreased perimetric mean sensitivity measured by Humphry visual field analyzer (program 10-2)
(3) Patients aged 50-year-old or more and can sign an informed consent form for participation of this study
(4) Patients whom the principal investigator judges competent
(5) Patients with no lutein allergy
(1) Eyes with cataract that affect the measurement of visual function tests.
(2) Eyes received cataract surgery within six months
(3) Eyes with glaucoma, diabetic retinopathy and any other eye disease
(4) Patient with serious disease in liver, kidney or heart that impacts on the evaluation of the use of lutein supplements
(5) Patient who is taking photosensitive medicine, such as phenothiazine, chloroquine or tetracycline
(6) Patient who involved in the other clinical trials within three months
(7) Others. Patients whom the principal investigator judges incompetent
80
1st name | |
Middle name | |
Last name | Akira Obana, MD, PhD |
Seirei Hamamatsu General Hospital
Department of Ophthalmology
2-12-12 Sumiyoshi, Hamamatsu, Shizuoka, 430-8558, Japan
053-430-2222
1st name | |
Middle name | |
Last name | Akira Obana, MD, PhD |
Seirei Hamamatsu General Hospital
Department of Ophthalmology
2-12-12 Sumiyoshi, Hamamatsu, Shizuoka, 430-8558, Japan
053-430-2222
obana@sis.seirei.or.jp
Raman Study Team
Seirei Hamamatsu General Hospital
Self funding
Japan
None
Kemin Japan, Koyo Mercantile Co., LTD
NO
2007 | Year | 03 | Month | 11 | Day |
Unpublished
Completed
2006 | Year | 12 | Month | 11 | Day |
2007 | Year | 03 | Month | 01 | Day |
2009 | Year | 03 | Month | 01 | Day |
2009 | Year | 09 | Month | 01 | Day |
2009 | Year | 09 | Month | 01 | Day |
2010 | Year | 07 | Month | 01 | Day |
2007 | Year | 03 | Month | 11 | Day |
2009 | Year | 09 | Month | 11 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000769