Dairy Modulation of Oxidative and Inflammatory Stress in Overweight and Obese Subjects
Completed · Not applicable
Conditions studied: Obesity, Overweight
In brief
The objective of this study is to determine the acute effects of a dairy supplement compared to a soy supplement on oxidative and inflammatory stress in overweight and obese subjects in the absence of any changes in adiposity.
Key facts
- Study ID
- NCT00948038
- Run by
- University of Tennessee
- People needed
- 20
- Starts
- 2007-01-01
- Expected to finish
- 2009-05-01
- Last updated by the study team
- 2009-07-29
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Body mass index (BMI) 25-29.9 (n=10); 30-34.9 kg/m2 (n=10)
- Age 18-50 years
- Weight stable: no more than 3 kg weight loss during past three months
You may not qualify if…
- BMI < 25 or >35
- Type II diabetes requiring the use of any oral antidiabetic agent and/or insulin (because of confounding effects on ROS)
- Adverse response to study foods (lactose intolerance, dairy intolerance, dairy allergy); this will be determined by self-report.
- history or presence of significant metabolic disease which could impact on the results of the study (i.e. endocrine, hepatic, renal disease)
- history of eating disorder
- presence of active gastrointestinal disorders such as malabsorption syndromes
- pregnancy or lactation
- use of obesity pharmacotherapeutic agents within the last 6 months
- use of over-the-counter anti-obesity agents (e.g. those containing phenylpropanalamine, ephedrine and/or caffeine) within the last 6 months
- Recent (current or past 12 weeks) use of any psychotropic medication
- Recent (past four weeks) initiation of an exercise program
- Recent (past twelve weeks) initiation of hormone replacement therapy or change in HRT regimen
- Recent (past twelve weeks) initiation of hormonal birth control or change in hormonal birth control regimen
- Recent (current or past 12 weeks) history of smoking
Where it is running
- The University of Tennessee — Knoxville, Tennessee, United States
Full record on ClinicalTrials.gov
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