The Effect of a Nutritional Supplement in Individuals With Type 2 Diabetes Mellitus: a Pilot Study
NCT ID: NCT01505803
Last Updated: 2012-01-09
Study Results
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Basic Information
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COMPLETED
PHASE1
48 participants
INTERVENTIONAL
2010-07-31
2011-12-31
Brief Summary
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Detailed Description
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This study will recruit 48 postmenopausal women with type 2 DM. Participants will be randomly allocated to one of 4 groups for a period of 12 weeks: placebo, zinc, omega 3, or zinc + omega 3 supplementation. Usual dietary intake will be assessed before and after the trial period using 2-day estimated food records, which will be checked by a research dietitian. Blood samples will be collected from all participants at the start of the intervention (week 0) then at 4 weekly intervals (weeks 4, 8, 12) by qualified phlebotomists. Blood samples will be analysed for plasma zinc, plasma lipids and fatty acids, markers of inflammation and oxidative stress, and indicators of glycaemic control. An aliquot of blood will also be used for the measurement of zinc transporter mRNA levels utilising real-time quantitative PCR techniques.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Zinc supplement
Zinc supplements
Participants will receive 40 mg of zinc each day for 12 weeks.
Placebo supplements
Participants will receive placebo supplements each day for 12 weeks.
Omega 3 supplement
Omega 3 supplements
Participants will receive 2 g of omega 3 fatty acids each day for 12 weeks.
Placebo supplements
Participants will receive placebo supplements each day for 12 weeks.
Zinc and omega 3 supplements
Zinc supplements
Participants will receive 40 mg of zinc each day for 12 weeks.
Omega 3 supplements
Participants will receive 2 g of omega 3 fatty acids each day for 12 weeks.
Placebo supplement
Placebo supplements
Participants will receive placebo supplements each day for 12 weeks.
Interventions
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Zinc supplements
Participants will receive 40 mg of zinc each day for 12 weeks.
Omega 3 supplements
Participants will receive 2 g of omega 3 fatty acids each day for 12 weeks.
Placebo supplements
Participants will receive placebo supplements each day for 12 weeks.
Eligibility Criteria
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Inclusion Criteria
* Type 2 diabetes (controlled by diet and lifestyle; or oral hypoglycaemic medication (i.e. metformin) for not more than 7 years)
* Normal Glomerular Filtration Rate (GFR) and normal microalbumin/creatine ratio
* No nutritional supplements in the 6 weeks prior to the trial \& continuing through the trial period
* Non-smoking
Exclusion Criteria
* Taking medications that are likely to interfere with zinc metabolism
48 Years
FEMALE
No
Sponsors
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University of Sydney
OTHER
Responsible Party
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Principal Investigators
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Samir Samman
Role: PRINCIPAL_INVESTIGATOR
University of Sydney
Meika Foster
Role: PRINCIPAL_INVESTIGATOR
University of Sydney
Locations
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University of Sydney
Sydney, New South Wales, Australia
Countries
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References
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Foster M, Petocz P, Samman S. Effects of zinc on plasma lipoprotein cholesterol concentrations in humans: a meta-analysis of randomised controlled trials. Atherosclerosis. 2010 Jun;210(2):344-52. doi: 10.1016/j.atherosclerosis.2009.11.038. Epub 2009 Nov 29.
Foster M, Samman S. Zinc and redox signaling: perturbations associated with cardiovascular disease and diabetes mellitus. Antioxid Redox Signal. 2010 Nov 15;13(10):1549-73. doi: 10.1089/ars.2010.3111.
Foster M, Hancock D, Petocz P, Samman S. Zinc transporter genes are coordinately expressed in men and women independently of dietary or plasma zinc. J Nutr. 2011 Jun;141(6):1195-201. doi: 10.3945/jn.111.140053. Epub 2011 Apr 13.
Other Identifiers
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HREC 12392
Identifier Type: -
Identifier Source: org_study_id
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