Can Fish Oil and Phytochemical Supplements Mimic Anti-Aging Effects of Calorie Restriction?
This study has been completed.
Sponsor:
Washington University School of Medicine
Collaborator:
Barnes-Jewish Hospital
Information provided by (Responsible Party):
Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT01752868
First received: December 14, 2012
Last updated: NA
Last verified: December 2012
History: No changes posted
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Purpose
The purpose of this study is to determine if a combination of 10 nutritional supplements provide health benefits that are consistent with protection against age-related disease. All supplements have been shown in previous studies to have health benefits when administered alone. The hypothesis is that 6 months of taking 10 nutritional supplements each day will provide beneficial changes in healthy related measures.
| Condition | Intervention |
|---|---|
|
Healthy Volunteers |
Dietary Supplement: Supplement |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Can Fish Oil and Phytochemical Supplements Mimic Anti-Aging Effects of Calorie Restriction? |
Resource links provided by NLM:
MedlinePlus related topics:
Dietary Supplements
Drug Information available for:
Fish oil
U.S. FDA Resources
Further study details as provided by Washington University School of Medicine:
Primary Outcome Measures:
- Carotid-femoral pulse wave velocity [ Time Frame: Baseline and 6 months ] [ Designated as safety issue: No ]
| Enrollment: | 56 |
| Study Start Date: | May 2011 |
| Study Completion Date: | August 2012 |
| Primary Completion Date: | August 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: supplement |
Dietary Supplement: Supplement
Participants in this group will take the following nutritional supplements on a daily basis: curcumin, fish oil, resveratrol, sesamin, Acetyl-L-carnitine, lipoic acid, green and black teas, quercetin, pomegranate, cinnamon bark.
|
| No Intervention: control |
Eligibility| Ages Eligible for Study: | 40 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- age 40-60 yr
- body mass index of 21 - 30 kg/m2
- sedentary to moderately active
- eating a typical US diet
Exclusion Criteria:
- history of any chronic disease other than mild osteoarthritis
- use of medications other than occasional use of non-steroidal anti-inflammatory drugs, antihistamines, antacids or laxatives
- use of nutritional supplements
- smoking
- alcohol intake greater than two drinks per day for women and three drinks per day for men
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01752868
Locations
| United States, Missouri | |
| Washington University Medical Center | |
| St. Louis, Missouri, United States, 63110 | |
Sponsors and Collaborators
Washington University School of Medicine
Barnes-Jewish Hospital
Investigators
| Principal Investigator: | Luigi Fontana, MD, PhD | Washington University School of Medicine |
More Information
No publications provided
| Responsible Party: | Washington University School of Medicine |
| ClinicalTrials.gov Identifier: | NCT01752868 History of Changes |
| Other Study ID Numbers: | BJH 6936-33 |
| Study First Received: | December 14, 2012 |
| Last Updated: | December 14, 2012 |
| Health Authority: | United States: Institutional Review Board |
ClinicalTrials.gov processed this record on May 21, 2013