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The Effects of the Food Preservative Propionic Acid in Post-prandial Metabolism

Pilot Study to Study the Effects of the Food Preservative Calcium Propionate on Postprandial Hormonal and Metabolic Milieu

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01889446
Acronym
Walnut
Enrollment
20
Registered
2013-06-28
Start date
2013-08-31
Completion date
2015-06-30
Last updated
2014-09-22

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

Conditions

Diabetes, Insulin Resistance, Obesity

Keywords

Propionic acid, Food preservatives

Brief summary

Propionic acid (PA) is used as a preservative in foods such as cheeses, baked goods, or additive for artificial fruit flavors. The U.S. Environmental Protection Agency considers it safe and therefore, has no limitation on its use. Since PA has been shown before to serve as a substrate for glucose production in the liver, the purpose of this study is to find out if PA intake causes changes in levels of glucose, insulin and other important hormones following a meal. This research study will compare PA to placebo. The placebo looks exactly like the active substance, but it does not contain any active agent (PA). Placebos are used in research studies to see if the results are due to the study drug or to other reasons. The investigators plan to have 20 subjects take part in this study at the Brigham and Women's Hospital (BWH).

Detailed description

-To test whether PA, added as food supplement to humans, results in altered post-prandial metabolism. The investigators propose to conduct a double-blind, randomized, placebo controlled, cross-over study in which blood levels of metabolites and hormones will be measured in healthy volunteers following a mixed meal test without or with PA. Study design: This is a double-blind, randomized, placebo controlled, cross-over study. Twenty volunteers who meet the inclusion/exclusion criteria will be randomized into two groups, provided with a mixed meal without or with calcium proprionate (also known as E282). A week later, participants will be provided with a mixed meal again, following cross-over of the groups. Blood will be collected at baseline, and every 30 minutes for 4 hours. Study Subjects: 20 healthy male and female volunteers (ages 18 to 65 years) with a body mass index (BMI) of 20 to \<30 Kg/m2.

Interventions

DIETARY_SUPPLEMENTCalcium propionate

Sponsors

Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-65 years * Good health as evidenced by history and physical exam * BMI: 20-29.9 kg/m2

Exclusion criteria

* Fasting plasma glucose \>110 mg/dL * HbA1c \>6.0% * Significant current illness other than treated hypothyroidism * BP \>135/85 or systolic BP \<90 mm Hg * Hepatic disease (transaminase \> 3 times normal) * Renal impairment (Creatinine clearance \<60 ml/min) * History of drug or alcohol abuse * Participation in any other concurrent clinical trial * Pregnant women * History of food allergies.

Design outcomes

Primary

MeasureTime frame
Post prandial insulin levelsDuring 4 hours after consumption of a meal

Countries

United States

Contacts

Primary ContactAmir Tirosh, MD PhD
ATIROSH@PARTNERS.ORG
Backup ContactKyle Carbone
kcarbone3@partners.org

Outcome results

None listed

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