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NCT03957239 · ClinicalTrials.gov registry record · NA
The Effect of a Cranberry Beverage on Intestinal Permeability and Gastrointestinal Function in Generally Healthy Adults
A NA study of Intestinal Permeability and Gastrointestinal Function, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 43
- Enrollment target
- 1
- Study location
NCT03957239 is a NA study of Intestinal Permeability and Gastrointestinal Function that has completed, run by University of Florida. The registered enrollment target is 43 participants, below the 51-participant average among 3 other Intestinal Permeability trials with a reported enrollment target (16% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03957239, a NA study of Intestinal Permeability and Gastrointestinal Function, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 43 participants
- Enrollment target
- 1
- Study location
Study Summary
In this double blind, crossover study participants will consume a cranberry beverage and a cranberry-flavored beverage for 2 weeks each. Gut permeability will be assessed weekly using aspirin and food-grade sugar molecules. Participants will be asked to provide urine, blood, saliva and stool samples to assess gut permeability and microbial communities. No change in permeability to the small sugar probes is anticipated with the cranberry beverage
Conditions Studied
Interventions
- OTHER Control Beverage
- OTHER Cranberry Beverage
Study Locations (1)
Florida
- UF Health at the University of Florida - Gainesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 43 participants |
| Start Date | 2019-09-05 |
| Est. Completion | 2020-01-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03957239
The ClinicalTrials.gov registry entry for NCT03957239 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 51-participant average among 3 other Intestinal Permeability trials with a reported enrollment target (16% lower). The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Intestinal Permeability appearing as the primary indexed condition, and to 2 interventions - of which Control Beverage is the first listed.
NCT03957239 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT03957239 about?
NCT03957239 is a clinical study titled "The Effect of a Cranberry Beverage on Intestinal Permeability and Gastrointestinal Function in Generally Healthy Adults". In this double blind, crossover study participants will consume a cranberry beverage and a cranberry-flavored beverage for 2 weeks each. Gut permeability will be assessed weekly using aspirin and food-grade sugar molecules. Participants will be asked to provide urine, blood, saliva and stool samples...
What is the current status of trial NCT03957239?
This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2019-09-05. Estimated completion is 2020-01-02.
What conditions does trial NCT03957239 study?
This clinical trial studies the following conditions: Intestinal Permeability, Gastrointestinal Function.
What interventions are being tested in trial NCT03957239?
The interventions under investigation include: Control Beverage (OTHER), Cranberry Beverage (OTHER).
Who is sponsoring clinical trial NCT03957239?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03957239 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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