Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02667184 · ClinicalTrials.gov registry record · NA
The Effect of a Low FODMAP Oral Nutrition Supplement On Breath Hydrogen Response In Healthy Human Subjects
A NA study of Food Selection, sponsored by University of Minnesota.
- Completed
- Registry status
- NA
- Development phase
- 21
- Enrollment target
- 1
- Study location
NCT02667184: Completed NA study of Food Selection, sponsored by University of Minnesota.
NCT02667184 is a NA study of Food Selection that has completed, run by University of Minnesota. The registered enrollment target is 21 participants, below the 818-participant average among 12 other Food Selection trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02667184, a NA study of Food Selection, has completed, sponsored by University of Minnesota.
- COMPLETED
- Registry status
- NA
- Development phase
- 21 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this study is to determine subjective gastrointestinal tolerance response and differences in breath hydrogen response following the consumption of different types of low FODMAP oral nutrition supplements. This randomized, crossover study requires participants to arrive to the lab 12 hours fasted, consume an oral liquid supplement and complete gastrointestinal tolerance questionnaires as well as produce samples for breath hydrogen analysis at various time points over a 4 hour time period.
Primary Outcome
At baseline, subjects will be asked to exhale a full breath into a sample collection bag. The breath samples will be extracted and measured using the Quintron Breath Track Analyzer. This will be a marker of carbohydrate fermentation in the colon.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Low FODMAP Oral Nutrition Supplement
Study Locations (1)
Minnesota
- University of Minnesota - Saint Paul
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2016-05 |
| Est. Completion | 2016-06 |
| Phase | NA |
What the finished NCT02667184 record still lists
NCT02667184 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 818-participant average among 12 other Food Selection trials with a reported enrollment target (97% lower).
The record links to 1 condition, with Food Selection appearing as the primary indexed condition, and to 1 intervention - of which Low FODMAP Oral Nutrition Supplement is the first listed.
NCT02667184 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT02667184 about?
NCT02667184 is a clinical study titled "The Effect of a Low FODMAP Oral Nutrition Supplement On Breath Hydrogen Response In Healthy Human Subjects". The goal of this study is to determine subjective gastrointestinal tolerance response and differences in breath hydrogen response following the consumption of different types of low FODMAP oral nutrition supplements. This randomized, crossover study requires participants to arrive to the lab 12 hour...
What is the current status of trial NCT02667184?
This trial is currently completed. It is a NA study. The enrollment target is 21 participants. The study started on 2016-05. Estimated completion is 2016-06.
What conditions does trial NCT02667184 study?
This clinical trial studies the following conditions: Food Selection.
What interventions are being tested in trial NCT02667184?
The interventions under investigation include: Low FODMAP Oral Nutrition Supplement (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT02667184?
This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02667184 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Food Selection
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02667184's enrollment target sits among peer trials
21 12th of 12 higher than 1 of 12 other Food Selection trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Food Selection 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
-
Increasing Food Literacy in Preschoolers to Reduce Obesity Risk
RECRUITING · NA
-
Integrating Food Rx With Best Feeding Practices With EFNEP
RECRUITING · NA
-
Influence of Social Media Ads on Food Choice - Master Protocol
RECRUITING · NA
-
The Florida ASCENT Study
RECRUITING · NA
-
Sleep and Metabolism
RECRUITING · NA
-
Influence of "Likes" in Social Media Food Ads on Black and White Adolescents' Food Purchases - Study 2
RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02447874 · 21 participants · Phase 1
Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease
- NCT03826992 · 21 participants · Phase 1
Venetoclax Combined With Vyxeos (CPX-351) for Participants With Relapsed or Refractory Acute Leukemia
- NCT04107077 · 21 participants · Phase 2
Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer
- NCT04158635 · 21 participants · Phase 1
Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic Cancer
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia