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NCT01187875 · ClinicalTrials.gov registry record · Early Phase 1
Resistant Starch and Satiety
A Early Phase 1 study, sponsored by University of Minnesota.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 20
- Enrollment target
NCT01187875: Completed Early Phase 1 study, sponsored by University of Minnesota.
NCT01187875 is a Early Phase 1 study that has completed, run by University of Minnesota. The registered enrollment target is 20 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01187875, a Early Phase 1 study, has completed, sponsored by University of Minnesota.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 20 participants
- Enrollment target
Study Summary
Dietary fiber consumption may contribute to weight regulation by improving satiety. In an earlier study the investigators found that a muffin containing resistant starch was more effective than other fibers in altering satiety. The objective of this study is to determine if 2 resistant starches consumed in muffins alter satiety and whether a mixture of resistant starches is more effective than either alone in enhancing satiety.
Primary Outcome
Satiety response was measured using subjective perceptions of hunger, fullness, satisfaction, and prospective food intake evaluated by previously validated visual analogue scales (VAS).
Interventions
- DIETARY_SUPPLEMENT Placebo- Fiber free control
- DIETARY_SUPPLEMENT Hi-maize resistant starch 9g
- DIETARY_SUPPLEMENT Novalose 330 resistant starch 9g
- DIETARY_SUPPLEMENT 4.5g Hi-maize resistant starch and 4.5g Novalose 330
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2009-09 |
| Est. Completion | 2011-06 |
| Phase | Early Phase 1 |
What the finished NCT01187875 record still lists
NCT01187875 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (62% lower).
The record links to 0 conditions, and to 4 interventions - of which Placebo- Fiber free control is the first listed.
NCT01187875 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01187875 about?
NCT01187875 is a clinical study titled "Resistant Starch and Satiety". Dietary fiber consumption may contribute to weight regulation by improving satiety. In an earlier study the investigators found that a muffin containing resistant starch was more effective than other fibers in altering satiety. The objective of this study is to determine if 2 resistant starches cons...
What is the current status of trial NCT01187875?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 20 participants. The study started on 2009-09. Estimated completion is 2011-06.
What interventions are being tested in trial NCT01187875?
The interventions under investigation include: Placebo- Fiber free control (DIETARY_SUPPLEMENT), Hi-maize resistant starch 9g (DIETARY_SUPPLEMENT), Novalose 330 resistant starch 9g (DIETARY_SUPPLEMENT), 4.5g Hi-maize resistant starch and 4.5g Novalose 330 (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT01187875?
This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01187875's enrollment target sits among peer trials
20 1157th of 2000 higher than 710 of 2,000 other Early Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Early Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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