Not Yet RecruitingNot Applicable

Probiotic Intervention in Constipation

30 participantsStarted 2026-04-01

Plain-language summary

To evaluate the effects of probiotic intervention on gastrointestinal function in patients with constipation after 4 weeks of treatment, and to explore its potential effects on immune status and bone metabolism.

Who can participate

Age range18 Years – 65 Years

SexALL

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Inclusion criteria

✓. Aged 18-65 years.
✓. Patients with constipation, defined as fewer than three bowel movements per week and/or Bristol Stool Form Scale (BSFS) types 1-2.
✓. Able to comply with the study protocol and complete the study procedures.
✓. Participants who have voluntarily signed the informed consent form.
✓. Participants (including male participants) must have no plans for pregnancy from 14 days before screening until 6 months after the end of the study and must agree to use effective contraception during this period.

Exclusion criteria

✕. Individuals who have recently taken products with similar functions to the investigational product that may affect the evaluation of study outcomes.
✕. Participants who plan to change their dietary habits during the study period.
✕. Patients with severe allergies or immunodeficiency.
✕. Women who are pregnant, breastfeeding, or planning to become pregnant.
✕. Patients with severe diseases of major organs such as the cardiovascular system, lungs, liver, or kidneys, or those with severe metabolic diseases (e.g., diabetes or thyroid disorders), malignant tumors, or severe immune system diseases.
✕. Individuals who have used antibiotics within the past two weeks.
✕. Individuals with severe psychological or psychiatric disorders.
✕. Participants who fail to take the investigational product as required or fail to attend scheduled follow-up visits, resulting in an inability to determine treatment efficacy.

What they're measuring

Changes in stool consistency

Timeframe: 8 weeks

Trial details

NCT IDNCT07462494

SponsorWecare Probiotics Co., Ltd.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2026-12-01

Contact for this trial

Ying Jin, Doctor

13375163966 sunny13211@sina.com

View on ClinicalTrials.gov More Gastrointestinal Function trials