Gut bacteria study aims to end constipation woes
NCT ID NCT07529457
First seen Jun 27, 2026 · Last updated Aug 28, 2026 · Updated 2 times
Summary
This study tests whether a probiotic called Akk09 can improve bowel movements and ease constipation symptoms in adults. About 70 participants will take either the probiotic or a placebo daily for 4 weeks. Researchers will track changes in stool consistency and overall gut health.
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 70 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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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: 1. Men and women aged between 18 and 65 years; 2. Participants presenting with constipation, characterized by \<3 spontaneous bowel movements per week or BSFS stool types 1-2; 3. Capable of following the study protocol and completing all required assessments; Individuals who have voluntarily signed the informed consent form; 4. No plans for pregnancy from at least 14 days prior to screening through 6 months after the study, with agreement to use reliable contraception methods. Exclusion Criteria: 1. Intake of similar functional products within a short period prior to enrollment that could influence study results; 2. Participants who significantly alter their habitual diet during the trial; 3. Individuals with severe allergic conditions or impaired immune function; 4. Women who are pregnant, lactating, or intending to conceive; 5. Patients with serious underlying diseases affecting major organs or metabolic systems; 6. Antibiotic treatment within 2 weeks before enrollment; 7. Individuals with severe mental or psychological disorders; 8. Non-compliance with study requirements, including improper intake or missed follow-ups; 9. Other subjects considered inappropriate for participation by the investigator.
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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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Suzhou Ninth People's Hospital
RECRUITINGSuzhou, Jiangsu, 215000, China
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