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Pilot Study: Herbs, Spices, and Glucose Response

This pilot study wants to see if a continuous glucose monitor (CGM) can accurately measure how your blood sugar changes after eating a potato dish, with or without a blend of herbs and spices. You might be able to join if you are between 18 and 50 years old, have a BMI between 20-35, don't have food allergies to the study items, and are willing to wear a CGM for at least 10 days. The study will look at your blood sugar levels at specific times after eating and over 24 hours. The study is currently unclear on its recruitment status and plans to enroll up to 10 participants.

Study design
This is a pilot study with a maximum of 10 participants. You will eat three different potato entrees, with the order of entrees being randomized.
What's involved
You will consume one specific entree per day over a 10-day period. You will also need to wear a continuous glucose monitor for at least 10 days.
Compensation
Not stated in the trial record.
Follow-up
Your post-meal glucose response will be measured at 0, 1, and 2 hours after eating, as well as continuously for 24 hours.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07254624

Pilot Assessment of Continuous Glucose Monitor for Post-meal Glucose Responses to Herbs and Spices.

Active, Not Recruiting
NAAges 18–50Interventional
University of Alabama at Birmingham
~10 participants
Updated 2026-06-09 on ClinicalTrials.gov
What's tested:Mix of five herbs and spicesPotato entree

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Post-prandial glucose response
Measured over 0, 1, and 2 hours post-meal, as well as 24 hour continuous

Conditions

Post-prandial Glucose Response

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Healthy Volunteers

NCT07254624

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of Alabama at Birmingham

    Birmingham, Alabamano site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

body mass index (BMI): 20-35
no dietary restriction or food allergies to study items
weight stable
access to a smart phone
willingness to wear a continuous glucose monitor for the duration of the study (at minimum 10 days)

Exclusion

pregnancy or anticipating pregnancy or lactation
food allergy to study items
diagnosed diabetes (type 1 or 2) or taking diabetes medications
history of bariatric surgery
consumed \>1 serving of potatoes daily before enrollment
5% weight loss or gain within the past 6 months
medical conditions or medication that would prevent the ability to comply with the treatment assignment and/or affect blood glucose or energy balance
condition which would prevent the ability to wear a continuous glucose monitor on the upper arm for the study duration

What this trial measures

  • Post-prandial glucose response0, 1, and 2 hours post-meal, as well as 24 hour continuous

    Glucose response will be measured using continuous glucose monitors. These devices will capture changes in glucose response from the start of the meal to about 2 hours postprandial.