Clinical Trials Directory

Trials / Completed

CompletedNCT00153764

Effectiveness of a Vitamin Mineral Supplement

Effectiveness of a One-a-Day Cooper Complete Vitamin / Mineral Supplement With or Without Omega-3 Fatty Acid Ingestion

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
75 (actual)
Sponsor
The Cooper Institute · Academic / Other
Sex
All
Age
30 Years – 70 Years
Healthy volunteers
Accepted

Summary

The goal of the study is to evaluate the effectiveness of a new one-a-day Cooper complete vitamin supplement with or without a combined omega-3 fatty acid supplement on selected clinical risk factor measures. Participants taking the Cooper Complete one-a-day vitamin plus omega-3 fatty acid will have greater improvement in homocysteine, LDL cholesterol, and C-reactive protein than those taking the other supplements.

Detailed description

Participants will be randomized to 1 of 3 groups: vitamin with omega-3, vitamin w/o omega-3, or omega-3 alone. They will take the vitamin 12 weeks, after which time they will return for all laboratory tests. Persons who are currently taking a supplement must undergo a 2-week washout period before beginning the study. Participants taking the Cooper Complete one-a-day vitamin plus omega-3 fatty acid will have greater improvement in homocysteine, LDL cholesterol, and C-reactive protein than those taking the other supplements.

Conditions

Interventions

TypeNameDescription
DRUGCooper Complete One-A-Day Vitamin Supplement

Timeline

Start date
2004-09-01
Primary completion
2006-03-01
Completion
2006-03-01
First posted
2005-09-12
Last updated
2012-08-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00153764. Inclusion in this directory is not an endorsement.

Effectiveness of a Vitamin Mineral Supplement (NCT00153764) · Clinical Trials Directory