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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00596024
Other study ID # LAD
Secondary ID Alzheimer resear
Status Terminated
Phase Phase 2
First received
Last updated
Start date December 2007
Est. completion date July 2009

Study information

Verified date August 2019
Source Oregon Health and Science University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Oxidative damage by free radicals may be involved in causing Alzheimer's disease (AD). Free radicals may lead to death of nerve cells and decline in brain function. Certain antioxidants may suppress this free radical damage associated with AD. Carotenoids are a family of naturally occurring antioxidants that have important functions for human health. Carotenoids are known to reduce oxidative damage, but their effects have not been studied in AD patients.

The objective of the study is to examine whether lutein supplementation helps to reduce oxidative damage from free radicals in AD patients.


Recruitment information / eligibility

Status Terminated
Enrollment 3
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender All
Age group 55 Years and older
Eligibility Inclusion Criteria:

- Diagnosed with moderately severe Alzheimer's disease

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
lutein/zeaxanthin
daily supplementation of lutein and zeaxanthin at dose of 12 mg/day
placebo
placebo capsules with the same size and coating as those of lutein/zeaxanthin supplements without active ingredients

Locations

Country Name City State
United States Oregon Health and Science University Portland Oregon

Sponsors (2)

Lead Sponsor Collaborator
Oregon Health and Science University Oregon Partnership for Alzheimer's Research

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary oxidative damage markers 3 months
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