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
24 participants
INTERVENTIONAL
2005-01-31
2008-05-31
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.
A Randomized Cross-over Trial of the Postprandial Effects of Three Different Diets in Patients With Type 2 Diabetes
NCT01522157
Observational Analysis of the Associational Between Dietary Factors and Postprandial Glucose Fluctuations
NCT07117188
Dietary Interventions in Prediabetes
NCT01729078
Effect of Low-glycemic Index Meals Intake on DM2 Women Under Metformin Therapy
NCT03165877
Glucose and Insulin Responses to Test Foods
NCT01671878
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.
PARALLEL
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
type 2 diabetic subjects
oral glucose load
oral ingestion of 13C labeled glucose
overweight healthy subjects
oral glucose load
oral ingestion of 13C labeled glucose
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
oral glucose load
oral ingestion of 13C labeled glucose
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Healthy for one group nd type 2 diabetic for the second group
* Age between 30 and 65 years old
* Total cholesterol \< or = 7 mmol/l and triglycerides \< or = 4 mmol/l
* For diabetic group: treated by metformin and/or sulfonylurea and/or thiazolidinedione and HbA1c \< 6%
* Stable weight over last 3 months
* Informed consent
Exclusion Criteria
* Participation in an other trial 2 months before starting this one
* Ward of court or under guardianship (sheltered adults)
* Person deprived of freedom by judicial or administrative decision
* Type 1 diabetes and type 2 diabetes treated bu insulin or acarbose
* Existence of a previously diagnosed pathology (other than type 2 diabetes)
* Previous gastro-intestinal pathology
* Treated by corticoids, anorexigens, weight loss medicines
* Alcoholism or severe tobacco consumption
30 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
LESAFFRE SA
UNKNOWN
Centre de Recherche en Nutrition Humaine Rhone-Alpe
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
CENTRE DE RECHERCHE EN NUTRITION HUMAINE RHONE ALPES
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Centre de Recherche En Nutrition Humaine Rhone Alpes
Lyon, , France
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.
CRNHRA-06-002
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.