- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03783637
Measuring Single-Serving Grain Intake
3 juillet 2019 mis à jour par: Janet Novotny, USDA Beltsville Human Nutrition Research Center
The primary objective of this study is to identify markers of a single meal of whole grain oat and whole grain wheat intake in humans.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
The aim of this study is to identify compounds that are found in blood and urine and are derived from a single meal of whole grain oat or whole grain wheat intake so that epidemiological studies can be conducted to provide more accurate associations between whole grain intake and health.
Type d'étude
Interventionnel
Inscription (Réel)
12
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
Maryland
-
Beltsville, Maryland, États-Unis, 20705
- USDA-ARS Beltsville Human Nutrition Research Center
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
21 ans à 75 ans (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- 21 to 75 years of age
- Voluntarily agree to participate and sign an informed consent form
Exclusion Criteria:
- Body weight less than 110 lbs.
- Have a body mass index below 19 or above 38 kg/m2
- Known (self-reported) allergy or adverse reaction to study foods
- Women who have given birth during the previous 12 months or who are pregnant/lactating or who plan to become pregnant during the study
- History of bariatric surgery or nutrient malabsorption disease (such as celiac disease), Crohn's disease, diabetes, or metabolic disorders that may interfere with the study
- History of certain cancer diagnosis or treatment in the last 3 years
- Smoking or use of tobacco products in the past 6 months
- Suspected or known strictures, fistulas or physiological/mechanical GI obstruction
- Use of certain medications or supplements (prescription or over-the-counter) that may interfere with the study objectives, including blood thinning medications
- Unable or unwilling to give informed consent or communicate with study staff
- Self-report of alcohol or substance abuse within the past 12 months and/or current treatment for these problems (long-term participation in Alcoholics Anonymous is not an exclusion)
- Other medical, psychiatric, or behavioral factors that in the judgment of the Principal Investigator may interfere with study participation or the ability to follow the intervention protocol
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Autre: Whole Grain Oat
Volunteers will consume a breakfast meal containing whole grain oats after 7 days of a whole grain free diet.
|
A meal containing whole grain oats
|
|
Autre: Whole Grain Wheat
Volunteers will consume a breakfast meal containing whole grain wheat after 7 days of a whole grain free diet.
|
A meal containing whole grain wheat
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Identification of unknown biomarkers of grain intake immediately after grain consumption
Délai: Day 8
|
Blood and Urine metabolomics profiling will be conducted.
Metabolomics refers to the complete set of small molecule metabolites.
The METLIN Metabolomics Database is a repository of such chemicals and contains over 75,000 entries, thus metabolomics is a very broad assessment.
Blood and urine will be broadly analyzed with mass spectrometers for metabolomics, and all ionizing compounds will be captured by the detector, which reports the ratio of mass of the compound to the charge (units: m/z which is mass to charge).
The mass-to-charges will be compared across different time points of collection, and appearance of mass-to-charges in some collections (but not found in others when grains were not consumed) will indicate a biomarker of grain intake.
|
Day 8
|
|
Identification of unknown biomarkers of grain intake a day after grain consumption
Délai: Day 9
|
Blood and Urine metabolomics profiling will be conducted.
Metabolomics refers to the complete set of small molecule metabolites.
The METLIN Metabolomics Database is a repository of such chemicals and contains over 75,000 entries, thus metabolomics is a very broad assessment.
Blood and urine will be broadly analyzed with mass spectrometers for metabolomics, and all ionizing compounds will be captured by the detector, which reports the ratio of mass of the compound to the charge (units: m/z which is mass to charge).
The mass-to-charges will be compared across different time points of collection, and appearance of mass-to-charges in some collections (but not found in others when grains were not consumed) will indicate a biomarker of grain intake.
|
Day 9
|
|
Identification of unknown biomarkers of grain intake 2 days after grain consumption
Délai: Day 10
|
Urine metabolomics profiling will be conducted.
Metabolomics refers to the complete set of small molecule metabolites.
The METLIN Metabolomics Database is a repository of such chemicals and contains over 75,000 entries, thus metabolomics is a very broad assessment.
Urine will be broadly analyzed with mass spectrometers for metabolomics, and all ionizing compounds will be captured by the detector, which reports the ratio of mass of the compound to the charge (units: m/z which is mass to charge).
The mass-to-charges will be compared across different time points of collection, and appearance of mass-to-charges in some collections (but not found in others when grains were not consumed) will indicate a biomarker of grain intake.
|
Day 10
|
|
Identification of unknown biomarkers of grain intake immediately after grain consumption
Délai: Day 34
|
Blood and Urine metabolomics profiling will be conducted.
Metabolomics refers to the complete set of small molecule metabolites.
The METLIN Metabolomics Database is a repository of such chemicals and contains over 75,000 entries, thus metabolomics is a very broad assessment.
Blood and urine will be broadly analyzed with mass spectrometers for metabolomics, and all ionizing compounds will be captured by the detector, which reports the ratio of mass of the compound to the charge (units: m/z which is mass to charge).
The mass-to-charges will be compared across different time points of collection, and appearance of mass-to-charges in some collections (but not found in others when grains were not consumed) will indicate a biomarker of grain intake.
|
Day 34
|
|
Identification of unknown biomarkers of grain intake a day after grain consumption
Délai: Day 35
|
Blood and Urine metabolomics profiling will be conducted.
Metabolomics refers to the complete set of small molecule metabolites.
The METLIN Metabolomics Database is a repository of such chemicals and contains over 75,000 entries, thus metabolomics is a very broad assessment.
Blood and urine will be broadly analyzed with mass spectrometers for metabolomics, and all ionizing compounds will be captured by the detector, which reports the ratio of mass of the compound to the charge (units: m/z which is mass to charge).
The mass-to-charges will be compared across different time points of collection, and appearance of mass-to-charges in some collections (but not found in others when grains were not consumed) will indicate a biomarker of grain intake.
|
Day 35
|
|
Identification of unknown biomarkers of grain intake 2 days after grain consumption
Délai: Day 36
|
Urine metabolomics profiling will be conducted.
Metabolomics refers to the complete set of small molecule metabolites.
The METLIN Metabolomics Database is a repository of such chemicals and contains over 75,000 entries, thus metabolomics is a very broad assessment.
Urine will be broadly analyzed with mass spectrometers for metabolomics, and all ionizing compounds will be captured by the detector, which reports the ratio of mass of the compound to the charge (units: m/z which is mass to charge).
The mass-to-charges will be compared across different time points of collection, and appearance of mass-to-charges in some collections (but not found in others when grains were not consumed) will indicate a biomarker of grain intake.
|
Day 36
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Blood glucose
Délai: Days 8 and 34
|
Blood glucose will be measured.
Blood glucose is reported in mmol/L.
|
Days 8 and 34
|
|
Serum insulin
Délai: Days 8 and 34
|
Serum insulin will be measured.
Serum insulin is reported in mIU/L.
|
Days 8 and 34
|
|
Serum c-peptide
Délai: Days 8 and 34
|
Serum c-peptide will be measured.
Serum c-peptide is reported in ng/ml.
|
Days 8 and 34
|
|
Non-esterified fatty acids in blood
Délai: Days 8 and 34
|
Non-esterified fatty acids will be measured in blood.
Non-esterified fatty acids are reported as mEQ/L.
|
Days 8 and 34
|
|
Triglycerides in blood
Délai: Days 8 and 34
|
Triglycerides will be measured.
Triglycerides are reported as mmol/L.
|
Days 8 and 34
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
13 mai 2019
Achèvement primaire (Réel)
19 juin 2019
Achèvement de l'étude (Réel)
19 juin 2019
Dates d'inscription aux études
Première soumission
11 décembre 2018
Première soumission répondant aux critères de contrôle qualité
18 décembre 2018
Première publication (Réel)
21 décembre 2018
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
5 juillet 2019
Dernière mise à jour soumise répondant aux critères de contrôle qualité
3 juillet 2019
Dernière vérification
1 juillet 2019
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- HS62 - Single Grain
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .