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NCT06427915 · ClinicalTrials.gov registry record · NA
Studying Glucose and Appetite Response With Alternatives to Soda Pop
A NA study, sponsored by Olipop, PBC.
- Completed
- Registry status
- NA
- Development phase
- 30
- Enrollment target
NCT06427915 is a NA study that has completed, run by Olipop, PBC. The registered enrollment target is 30 participants.
The verdict
NCT06427915, a NA study, has completed, sponsored by Olipop, PBC.
- COMPLETED
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
Study Summary
The primary aim of this clinical trial is to determine the acute effects of OLIPOP (a lower sugar, high fiber prebiotic soda) consumption, compared to consumption of a commercially available sugar-sweetened soda pop, on blood glucose in response to the beverages alone and in combination with a carbohydrate-rich mixed lunch meal in free-living, generally healthy adults.This study will consist of one screening/randomization clinic visit (day 0) and one follow-up clinic visit (day 5), with participants consuming study products on their own (e.g., at home) following an assigned treatment sequence on days 1, 2, 3, and 4. The main questions answered by this trial are the impacts of a prebiotic rich soda versus a traditional soda on: 1) blood glucose levels with and without a meal, 2) perceived hunger levels, 3) perceived alertness levels and 4) total caloric intake.
Interventions
- OTHER OLIPOP prebiotic soda
- OTHER Traditional sugar-sweetened cola
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2024-05-15 |
| Est. Completion | 2024-06-21 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06427915
The ClinicalTrials.gov registry entry for NCT06427915 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Olipop, PBC, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which OLIPOP prebiotic soda is the first listed.
NCT06427915 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06427915 about?
NCT06427915 is a clinical study titled "Studying Glucose and Appetite Response With Alternatives to Soda Pop". The primary aim of this clinical trial is to determine the acute effects of OLIPOP (a lower sugar, high fiber prebiotic soda) consumption, compared to consumption of a commercially available sugar-sweetened soda pop, on blood glucose in response to the beverages alone and in combination with a carbo...
What is the current status of trial NCT06427915?
This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2024-05-15. Estimated completion is 2024-06-21.
What interventions are being tested in trial NCT06427915?
The interventions under investigation include: OLIPOP prebiotic soda (OTHER), Traditional sugar-sweetened cola (OTHER).
Who is sponsoring clinical trial NCT06427915?
This trial is sponsored by Olipop, PBC, which has 2 total clinical trials registered on ClinicalTrials.gov.
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