RecruitingNot ApplicableNCT07081100
Probiotics and Non-Organic Gastrointestinal Improvement
Study on the Effect of Probiotics on Improving Gastrointestinal Function in Patients With Non-organic Gastrointestinal Dysfunction
Sponsor
Wecare Probiotics Co., Ltd.
Enrollment
50 participants
Start Date
Aug 5, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
To verify the improvement of gastrointestinal function in patients with non-organic gastrointestinal dysfunction after 4 weeks of intervention with compound probiotics.
Eligibility
Min Age: 18 YearsMax Age: 65 Years
Inclusion Criteria4
- Voluntarily sign the informed consent form and agree to participate in the study.
- Ability to complete the study according to the trial protocol requirements.
- Aged 18-65 years.
- Clinical diagnosis of non-organic gastrointestinal dysfunction (e.g., functional dyspepsia, functional constipation) without other serious organic diseases.
Exclusion Criteria8
- Use of drugs affecting intestinal flora (antibiotics, probiotics, intestinal mucosal protectants, herbal medicines, etc.) for >1 week within 1 month prior to screening.
- Short-term use of products with functions similar to the investigational product, which may interfere with result interpretation.
- Antibiotic use during the study period.
- History of severe systemic diseases or malignancies.
- Allergy to any ingredient in the compound probiotic freeze-dried powder used in the trial.
- Pregnancy, lactation, or plans for pregnancy in the near future.
- Inability to participate due to personal reasons.
- Other conditions deemed unsuitable by the investigators.
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Interventions
DIETARY_SUPPLEMENTProbiotic group
Participants took a freeze-dried probiotic powder every day, half an hour after a meal.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07081100