Interactions Between Diet, Microbiome and Abiotic Conditions in the Gut
NCT ID: NCT04804319
Last Updated: 2024-12-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
63 participants
OBSERVATIONAL
2021-04-13
2021-11-29
Brief Summary
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Detailed Description
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On day 2 and day 9, participants will arrive fasting at the department in the morning and have their anthropometry, breath hydrogen and methane levels measured, and a blood sample will be collected from each participant.
The first visit (day 2) also includes a standardized meal test (rye bread, butter, jam, egg, and yogurt with nuts and berries) and intake of paracetamol (250 mg). Subsequently, the participants will stay at the department for the following 6 hours and have their postprandial breath hydrogen and methane measured and urine collected at specific intervals.
Moreover, a sub-set of the participants will on the first visit (day 2) immediately after intake of the standardized meal swallow a single-use gastrointestinal SmartPill capsule, which will monitor their gastrointestinal pH, transit time, temperature and pressure.
Conditions
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Keywords
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Study Design
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OTHER
OTHER
Interventions
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9-days habitual diet
9-days study with habitual diet including one standardized breakfast on a single day
Eligibility Criteria
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Inclusion Criteria
* Willing to daily collect a urine and stool sample at home and able to store them in their own freezer in a provided containers throughout the 9-days trial
* Willing to eat sweet corn and report corn-intestinal transit time questionnaire
* Willing to record 9 days dietary intake and defecation pattern
* Willing to have blood samples drawn two times
* Owns a device with access to the internet and is willing to use myfood24 platform
* Known ability to tolerate paracetamol and willing to consume ½ paracetamol tablet dissolved in water (250mg)
* Willing to eat rye bread, butter, jam, egg, yoghurt, berries and nuts
Exclusion Criteria
* Pregnant or lactating women
* Suffering from inflammatory bowel syndrome (IBS), small intestinal bacterial overgrowth (SIBO) or inflammatory bowel diseases (IBD)
* Intake of antibiotics, diarrhea inhibitors and laxatives ˂ 1month
* Current chronic or infectious diseases
* Diagnosis of diabetes
* History of cancer within the past 5 years (except adequately-treated localized basal cell skin cancer or in situ uterine cervical cancer)
* Frequent intake of painkillers or other medication (mild antidepressants and contraceptive pills are allowed)
* Concurrent participation in another trial
* Intake of medications potentially altering gastric pH (proton pump inhibitors, histamine receptor antagonists, antacids)
* Intake of medications potentially altering the gastrointestinal motility (prokinetics, antiemetic agents, anticholinergic agents, narcotic analgetics, nonsteroidal anti-inflammatory drugs)
* Dysphagia
18 Years
75 Years
ALL
Yes
Sponsors
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Technical University of Denmark
OTHER
KU Leuven
OTHER
University of Minnesota
OTHER
University of Copenhagen
OTHER
Responsible Party
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Henrik Munch Roager
Associate Professor
Locations
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University of Copenhagen, Department of Nutrition, Exercise and Sports
Copenhagen, , Denmark
Countries
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References
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Prochazkova N, Laursen MF, La Barbera G, Tsekitsidi E, Jorgensen MS, Rasmussen MA, Raes J, Licht TR, Dragsted LO, Roager HM. Gut physiology and environment explain variations in human gut microbiome composition and metabolism. Nat Microbiol. 2024 Dec;9(12):3210-3225. doi: 10.1038/s41564-024-01856-x. Epub 2024 Nov 27.
Other Identifiers
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M237
Identifier Type: -
Identifier Source: org_study_id