Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

The Effect of Continuous Sipping of a Glucose Solution on Markers of Oxidation in Men and Women (AOGI)

11. mars 2013 oppdatert av: Thomas Wolever, University of Toronto
The objective of this study is to determine the effect of reducing the rate of glucose absorption on oxidative stress after eating and to compare it with the effects of vitamin C. The hypothesis is that reducing the rate of glucose absorption will reduce oxidative stress to a similar extent as 1g vitamin C.

Studieoversikt

Detaljert beskrivelse

Recently, much attention has been paid to evidence that abnormalities of the postprandial state (hyperglycemia) are important contributing factors to the development of chronic disease. This attention has increased interest in the role low glycemic index (GI) foods could potentially play in preventing postprandial oxidative burst/stress. GI is a means by which to categorize carbohydrate according to their postprandial glycemic response. Low GI foods promote slow intestinal absorption, prolonged and less pronounced postprandial glycemia, may decrease risk of chronic disease, as well as provide metabolic benefit to people living with glucose abnormalities as well as those with normal glucose. Few studies have been conducted looking at the potential relationship between GI and oxidation and are limited by dietary/lifestyle confounders. The proposed study has been developed to eliminate these confounders. Hypotheses (3): 1. Sipping glucose slowly over 3h will result in less oxidative stress than ingesting the same amount of glucose as a bolus over 5min. 2. Sipping glucose will reduce oxidative stress to the same extent as 1g of oral vitamin C. 3. The effect of sipping glucose on oxidative stress will occur sooner than that of vitamin C.

Studietype

Intervensjonell

Registrering (Faktiske)

18

Fase

  • Ikke aktuelt

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

18 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • healthy males or females
  • 18 to 75 years

Exclusion Criteria:

  • diabetes
  • recent hospitalization

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Grunnvitenskap
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: Glucose bolus alone
50g glucose dissolved in water and consumed within 5 minutes.
50g anhydrous glucose dissolved in 300ml water consumed within 10min followed by a lunch (cheese sandwich, fruit and milk) at 4h.
Eksperimentell: Glucose sipping alone
50g glucose dissolved in water and consumed gradually over 3 hours.
50g anhydrous glucose dissolved in 300ml water consumed at rate of 25ml per 15min followed by a lunch (cheese sandwich, fruit and milk) at 4h.
Aktiv komparator: Glucose bolus plus 1g vitamin C
50g glucose dissolved in water and consumed in 5 minutes with 1g vitamin C
50g anhydrous glucose dissolved in 300ml water consumed within 10min with 1g vitamin C followed by a lunch (cheese sandwich, fruit and milk) at 4h.
Eksperimentell: Glucose sipping plus 1g vitamin C
50g glucose dissolved in water and consumed gradually of 3 hours. In addition 1g vitamin C will be taken with the first mouthful of glucose solution.
50g anhydrous glucose dissolved in 300ml water consumed at rate of 25ml per 15min. 1g vitamin C taken with first 25ml. Followed by a lunch (cheese sandwich, fruit and milk) at 4h.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Incremental Area Under the Curve over 4 hours in serum TRAP (total peroxyl radical-trapping potential)
Tidsramme: Four (4) hours after starting to eat the test meal.
Four (4) hours after starting to eat the test meal.

Sekundære resultatmål

Resultatmål
Tidsramme
Change over 6 hours from baseline in Plasma glucose
Tidsramme: Baseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Baseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Change over 6 hours from baseline in Plasma insulin
Tidsramme: Baseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Baseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Change over 6 hours from baseline in Plasma free-fatty acids
Tidsramme: Baseline and hourly for 6h
Baseline and hourly for 6h
Change over 6 hours from baseline in Serum vitamin C
Tidsramme: Baseline and 2, 4 and 6h
Baseline and 2, 4 and 6h
Change over 6 hours from baseline in C-reactive protein
Tidsramme: Baseline and 2, 4 and 6h
Baseline and 2, 4 and 6h
Change over 6 hours from baseline in Blood pressure
Tidsramme: Baseline and 1, 2, 4, 5 and 6h
Baseline and 1, 2, 4, 5 and 6h
Change over 6 hours from baseline in Pulse
Tidsramme: Baseline and 1, 2, 4, 5 and 6h
Baseline and 1, 2, 4, 5 and 6h
Change over 6 hours from baseline in Pulse pressure
Tidsramme: Baseline and 1, 2, 4, 5 and 6h
Baseline and 1, 2, 4, 5 and 6h
Change over 6 hours from baseline in Augmentation index
Tidsramme: Baseline and 1, 2, 4, 5 and 6h
Baseline and 1, 2, 4, 5 and 6h
Change over 6 hours from baseline in Oxidized LDL
Tidsramme: Baseline and hourly for 6hr
Baseline and hourly for 6hr
Change from baseline in serum TRAP over 6 hours
Tidsramme: Baseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Baseline and 30, 60, 120, 180, 240, 270, 300 and 360min

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Thomas MS Wolever, BMBCh PhD DM, University of Toronto
  • Studieleder: Shannan Grant, MSc, RD, University of Toronto

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

1. august 2010

Primær fullføring (Faktiske)

1. juni 2011

Studiet fullført (Faktiske)

1. juni 2011

Datoer for studieregistrering

Først innsendt

3. august 2011

Først innsendt som oppfylte QC-kriteriene

23. september 2011

Først lagt ut (Anslag)

27. september 2011

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

12. mars 2013

Siste oppdatering sendt inn som oppfylte QC-kriteriene

11. mars 2013

Sist bekreftet

1. mars 2013

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på glucose bolus

3
Abonnere