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NCT02831738 · ClinicalTrials.gov registry record · NA
Fiber Effects on Glycemic Index
A NA study, sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT02831738 is a NA study that has completed, run by Clinical Nutrition Research Center, Illinois Institute of Technology. The registered enrollment target is 20 participants.
The verdict
NCT02831738, a NA study, has completed, sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
Primary outcome measure: Changes in plasma glucose concentration over a 3 hour postprandial visit after administration of polydextrose (12g) compared to 0 mg placebo. Secondary outcome measure: Changes in gastrointestinal tolerance and acute bowel changes in 3 days following treatment administration.
Interventions
- DIETARY_SUPPLEMENT Polydextrose
- DIETARY_SUPPLEMENT Control Treatment
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2016-07-02 |
| Est. Completion | 2016-10-25 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02831738
The ClinicalTrials.gov registry entry for NCT02831738 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Clinical Nutrition Research Center, Illinois Institute of Technology, which has 59 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Polydextrose is the first listed.
NCT02831738 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02831738 about?
NCT02831738 is a clinical study titled "Fiber Effects on Glycemic Index". Primary outcome measure: Changes in plasma glucose concentration over a 3 hour postprandial visit after administration of polydextrose (12g) compared to 0 mg placebo. Secondary outcome measure: Changes in gastrointestinal tolerance and acute bowel changes in 3 days following treatment administratio...
What is the current status of trial NCT02831738?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2016-07-02. Estimated completion is 2016-10-25.
What interventions are being tested in trial NCT02831738?
The interventions under investigation include: Polydextrose (DIETARY_SUPPLEMENT), Control Treatment (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT02831738?
This trial is sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology, which has 59 total clinical trials registered on ClinicalTrials.gov.
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