Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
100 participants
INTERVENTIONAL
2011-12-31
2012-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of Advanced Glycation Endproducts on Satiety and Inflammation
NCT01434407
The Impact of Reformulated Foods on Cardiovascular Risk Factors
NCT01645995
Elucidation and Monitoring Postprandial Endothelial Function
NCT00766623
Ultra-processed Food Consumption, Gut Microbiota, and Glucose Homeostasis
NCT05358171
Burger and Beetroot Study - Lipid Oxidation Study
NCT02169661
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
low AGE, glucose
Food prepared by boiling/steaming and 20 g of glucose 3 times a day in a water solution
Dietary intervention
Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution
low AGE, fructose
Food prepared by boiling/steaming and 20 g of fructose 3 times a day in a water solution
Dietary intervention
Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution
high AGE, fructose
Food prepared by frying/baking and 20 g of fructose 3 times a day in a water solution
Dietary intervention
Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution
high AGE, glucose
Food prepared by frying/baking and 20 g of glucose 3 times a day in a water solution
Dietary intervention
Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Dietary intervention
Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* BMI between 25 and 40 kg/m2
* weight circumference over 88 cm
Exclusion Criteria
* Physical activity more than 8 h per week
* smoking
* medications and supplements
* being vegetarian or vegan
* pregnancy or breast feeding
* postmenopause
* chronic disease
* previous gastric bypass surgery
* blood donation within the last 3 months
* Involvement in other clinical trials
* allergic to paraaminobenzoic acid
20 Years
50 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
The Ministry of Science, Technology and Innovation, Denmark
OTHER_GOV
University of Copenhagen
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
AAstrup
Head of Department
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Susanne G Bugel
Role: PRINCIPAL_INVESTIGATOR
Department of Human Nutrition, University of Copenhagen
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Human Nutrition, University of Copenhagen
Frederiksberg, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
M201
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.