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Lactose, Sucrose & Corn Syrup Tolerance

Lactose: A Unique Carbohydrate Enabling Homeostatic Regulation of Blood Glucose & Insulin

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01789307
Enrollment
16
Registered
2013-02-12
Start date
2013-01-01
Completion date
2013-06-01
Last updated
2026-04-13

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

Conditions

Focus of Study: Oral Tolerance Test With Glucose, Lactose, Sucrose

Brief summary

Lactose, one of the key nutrients in human milk may be critically important to infants for more reasons than being a source of energy. We are interested in understanding how lactose when compared to other sugars influences how nutrients, specifically macronutrients are handled after digestion and absorption. To date, there have been no studies looking at how fat and protein varies when lactose compared to other sugars is ingested. There may be metabolic advantages to considering lactose for nutrition support of premature infants rather than glucose or dextrose as is often used in intravenous feeds, or the corn syrup solids in lactose-free formulas. We hope the information from this study will provide new information on the unique aspects of lactose. Hypothesis: The hypothesis is that providing carbohydrate as lactose: 1. minimizes the amount of carbohydrate that is converted into fat 2. enables a relatively constant metabolic state throughout feeding interval that avoids swings of high to low insulin, glucose, and fats.

Interventions

DIETARY_SUPPLEMENTcorn syrup solids

oral ingestion 50 grams, 2 doses

DIETARY_SUPPLEMENTsucrose

oral ingestion 50 grams, 2 doses

Sponsors

University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
19 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* male * at least 19 years of age * body mass index (BMI) between 18.5 and 25 * fasting blood glucose level \< 6.1 mmol/L (110 mg/dL) measured by glucometer on the day of the study and * comfortable speaking, reading and understanding English * comfortable drinking at least one cup (250 ml) of milk * non-smoking

Exclusion criteria

* not willing to provide blood samples, have * impaired lactose or glucose tolerance, * pre-diabetes, diabetes mellitus and any other endocrine disorder, * coronary heart disease, liver function test abnormalities or any chronic disease * routinely take medications, including aspirin, cyclooxygenase-2 inhibitors, statins and fish oil * consuming more than 1 alcoholic drink per day

Design outcomes

Primary

MeasureTime frameDescription
Postprandial changes in plasma insulin, glucagon, triglycerides and amino acids.6 hoursArea under the curve changes in the outcome measures following oral ingestion.

Secondary

MeasureTime frameDescription
Postprandial changes in plasma fatty acids.6 hoursArea under the curve analyses of changes in plasma fatty acids following oral ingestion

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORSheila M Innis, PhD

University of British Columbia, Child & Family Research Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026