- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03783637
Measuring Single-Serving Grain Intake
3. juli 2019 oppdatert av: 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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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.
Studietype
Intervensjonell
Registrering (Faktiske)
12
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Maryland
-
Beltsville, Maryland, Forente stater, 20705
- USDA-ARS Beltsville Human Nutrition Research Center
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
21 år til 75 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
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
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Annen: 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
|
|
Annen: 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
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Identification of unknown biomarkers of grain intake immediately after grain consumption
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Blood glucose
Tidsramme: Days 8 and 34
|
Blood glucose will be measured.
Blood glucose is reported in mmol/L.
|
Days 8 and 34
|
|
Serum insulin
Tidsramme: Days 8 and 34
|
Serum insulin will be measured.
Serum insulin is reported in mIU/L.
|
Days 8 and 34
|
|
Serum c-peptide
Tidsramme: 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
Tidsramme: 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
Tidsramme: Days 8 and 34
|
Triglycerides will be measured.
Triglycerides are reported as mmol/L.
|
Days 8 and 34
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
13. mai 2019
Primær fullføring (Faktiske)
19. juni 2019
Studiet fullført (Faktiske)
19. juni 2019
Datoer for studieregistrering
Først innsendt
11. desember 2018
Først innsendt som oppfylte QC-kriteriene
18. desember 2018
Først lagt ut (Faktiske)
21. desember 2018
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
5. juli 2019
Siste oppdatering sendt inn som oppfylte QC-kriteriene
3. juli 2019
Sist bekreftet
1. juli 2019
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- HS62 - Single Grain
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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