Clinical TrialID 5842

Assessment of Satiety Following Oral Administration of an Erythritol Sweetened Beverage

NCT02934321

Satiety in Healthy Volunteers

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Trial: 1Ingredient: 1Links: 1
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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
5842
Evidence Id
5842
Core Evidence Id
5842
Source Clinical Trial Id
5826
Herb2 Clinical Trial Id
HBCT005826
Nct Id
NCT02934321
Title
Assessment of Satiety Following Oral Administration of an Erythritol Sweetened Beverage
Status
Completed
Phase
Study Result
No
Study Condition
Satiety in Healthy Volunteers
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: PREVENTION
Intervention
DIETARY_SUPPLEMENT: Erythritol|DIETARY_SUPPLEMENT: Aspartame
Intervention Allocation
Randomized
Intervention Model
Crossover
Intervention Mask
Quadruple
Intervention Purpose
Prevention
Gender
All
Age
Adult
Enrollment
12
Outcome Measure
Ghrelin taken over 2 hours post beverage total area under curve (AUC), 0 min, 5 min, 10 min, 15 min, 20 min, 30 min, 45 min, 60 min, 75 min, 90 min, 120 min following consumption of test drink
Sponsor Collaborator
University of Florida
Funded By
OTHER
Location
University of Florida Clinical Research Center, Gainesville, Florida, 32610, United States
Other Id
IRB201601141
Start Date
2017-09-18
Primary Completion Date
2019-08-23
Completion Date
2019-08-23
First Posted
2016-10-14
Results First Posted
Last Update Posted
2019-08-28
Study Document
Study Url
https://clinicaltrials.gov/study/NCT02934321
Title Cn
Title En
Assessment of Satiety Following Oral Administration of an Erythritol Sweetened Beverage
Bilingual Status
semi_complete