Skip to content

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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01440790
Acronym
AOGI
Enrollment
18
Registered
2011-09-27
Start date
2010-08-31
Completion date
2011-06-30
Last updated
2013-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease, Diabetes

Brief summary

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.

Detailed description

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.

Interventions

DIETARY_SUPPLEMENTglucose bolus

50g anhydrous glucose dissolved in 300ml water consumed within 10min followed by a lunch (cheese sandwich, fruit and milk) at 4h.

DIETARY_SUPPLEMENTGlucose sipping

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.

DIETARY_SUPPLEMENTGlucose bolus plus 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.

DIETARY_SUPPLEMENTGlucose sipping plus 1g vitamin C

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.

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
University of Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy males or females * 18 to 75 years

Exclusion criteria

* diabetes * recent hospitalization

Design outcomes

Primary

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

Secondary

MeasureTime frame
Change over 6 hours from baseline in Plasma glucoseBaseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Change over 6 hours from baseline in Plasma insulinBaseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Change over 6 hours from baseline in Serum vitamin CBaseline and 2, 4 and 6h
Change over 6 hours from baseline in C-reactive proteinBaseline and 2, 4 and 6h
Change over 6 hours from baseline in Blood pressureBaseline and 1, 2, 4, 5 and 6h
Change over 6 hours from baseline in Plasma free-fatty acidsBaseline and hourly for 6h
Change over 6 hours from baseline in Pulse pressureBaseline and 1, 2, 4, 5 and 6h
Change over 6 hours from baseline in Augmentation indexBaseline and 1, 2, 4, 5 and 6h
Change over 6 hours from baseline in Oxidized LDLBaseline and hourly for 6hr
Change from baseline in serum TRAP over 6 hoursBaseline and 30, 60, 120, 180, 240, 270, 300 and 360min
Change over 6 hours from baseline in PulseBaseline and 1, 2, 4, 5 and 6h

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026