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Dietary Advanced Glycation End-products and Insulin Resistance in Overweight and Obese Humans

Will Reduction in Dietary Advanced Glycation End- Products Reduce Chronic Low Grade Inflammation and Improve Insulin Sensitivity in Overweight and Obese Humans

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00422253
Enrollment
27
Registered
2007-01-15
Start date
2006-11-30
Completion date
2012-12-31
Last updated
2013-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insulin Resistance, Obesity, Type 2 Diabetes

Keywords

insulin resistance, insulin secretion, advanced glycation end-products

Brief summary

We hypothesize that reduction in dietary advance glycation endproducts (AGE) intake will increase insulin sensitivity and normalise insulin secretion in overweight and obese individuals through reduction of chronic low grade inflammation. We propose to test this hypothesis by performing euglycemic hypeinsulinemic glucose clamp and intravenous glucose tolerance test before and after low AGE diet and normal Australian diet in a cross-over design. This study will provide information relevant to the development and prevention of type 2 diabetes.

Interventions

BEHAVIORALdietary intervention

Sponsors

Bayside Health
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* weight stable overweight and obese (BMI ≥ 25kg/m2) non-diabetic individuals, aged 18-50 years and healthy according to medical history, blood biochemistry and physical examination.

Exclusion criteria

* Participants will be excluded if they: * are aged \<18 years or \> 50 years; * currently smoke, have high alcohol use; or a positive urine drug screening test; * have a history of: diabetes, cardiovascular and hematological disease, respiratory, gastrointestinal, endocrine, renal or central nervous system disease, psychosis or psychiatric disorder, active cancer within last 5 years. * are actively seeking to lose weight, or if their weight has changed by more than 10 kilograms in the previous 12 months. * have been taking medication within one month prior to commencing the study; * have acute inflammation (by history, physical or laboratory examination) * are on hormonal contraceptives, or pregnant (by HCG urine pregnancy screening test) or lactating * have highly unusual dietary habits or follow vegan diets (because of the difficulty in complying with the assigned diet). * have current diabetes (determined by history and/or 75g glucose OGTT) * are unable to provide informed consent

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026