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