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Amyloid ß levels in human red blood cells

Amyloid ß levels in human red blood cells: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN42483402
Enrollment
62
Registered
2012-08-01
Start date
2010-06-01
Completion date
Unknown
Last updated
2017-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Astaxanthin supplementation study Not Applicable

Interventions

1. Higher astaxanthin content group: Ingesting supplement containing 1mg astaxanthin 2. Lower astaxanthin content group: Ingesting supplement containing 3mg astaxanthin 3. Control group: placebo Tota

Sponsors

Yamaha Motor Co., Ltd (Japan)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male and female, aged 20-69 2. Blood Test Value: Total Cholesterol: 200-260mg/dL or low density lipoprotein (LDL)-cholesterol: 120-180mg/dL

Exclusion criteria

Exclusion criteria: 1. All subjects who are capable to cause serious allergy symptoms to foods and medical drugs 2. They ingest medical drugs or herbal medicines which will affect result of test 3. They continuously ingest foods prepared with astaxanthin during past one month or even today 4. They regularly ingest health foods and beverages which profess similar effects with test foods 5. They drink alcohol more four or more days per week in the past three months 6. They have a history of circulatory disease, nephritis and hepatitis 7. They have digestive disease or have experienced the surgery of the digestive organs (except of surgery of appendicitis) 8. They exceed more than 2.5 of the standard value of Aspartate transaminase (AST), Alanine aminotransferase (ALT ) and gamma-glutamyltranspeptidase (?-GT) 9. They exceed more than 9.0 ml/g of the uric acid 10. They have serious anemia 11. They participate in other clinical trial with human subjects 12. They are judged by the principal investigator to participate in this clinical trial

Design outcomes

Primary

MeasureTime frame
1. Biological Antioxidant Potential (BAP) test 2. Determination of Reactive Oxygen Metabolites (d-ROMs) test Measured at Visit 1: Screening, Visit 2: Week 1, Visit 3: Weeks 4, Visit 4: Weeks 12

Secondary

MeasureTime frame
Peroxidized phospholipid measured at Visit 1: Screening, Visit 2: Week 1, Visit 3: Weeks 4, Visit 4: Weeks 12

Countries

Japan

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 25, 2026