Can fiber powders ease constipation? new study seeks answers
NCT ID NCT07202481
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether taking psyllium or fructooligosaccharide (two types of fiber) for six days improves bowel function in women with constipation. Twenty-five women will try each fiber and a control, keeping a diary and having a scan to measure how fast food moves through their gut. The goal is to see which fiber works better and if they cause side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- psyllium powder and fructooligosaccharide (dietary fibers)
- What this could lead to
- If it works, this could show that simple fiber supplements help women with constipation have more regular bowel movements.
- What could go wrong
- This is a very small, short-term study (25 women, 6 days per fiber). Results may not apply to everyone, and fibers can cause bloating or gas.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 59 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Female participants aged 18-59 years. * Willingness to sign the Informed Consent Form . * No restrictions on the consumption of egg or gluten. * No history or diagnosis of gastrointestinal diseases other than functional constipation. * Non-smokers. * No use of prebiotics, probiotics, synbiotics, or antibiotics at least 10 days prior to the study. * No previous surgery affecting gastrointestinal transit. * Willingness to discontinue the use of laxatives at least 4 days prior to scintigraphic imaging. * Participants who do not consume adequate dietary fiber (25-30 g/day) as assessed by dietary recall. * No confirmed or suspected pregnancy during the study. * No self-reported menopause Exclusion Criteria * Diagnosis of diabetes, severe hyperthyroidism, or hypothyroidism. * Use of opioid medications. * Delayed gastric emptying at 4 hours during the placebo period (participants meeting this criterion will be excluded from final analysis).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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School of Nursing, Federal University of Minas Gerais
RECRUITINGBelo Horizonte, Minas Gerais, 30130-100, Brazil
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