Probiotics and Non-Organic Gastrointestinal Improvement

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorWecare Probiotics Co., Ltd.

About this trial

To verify the improvement of gastrointestinal function in patients with non-organic gastrointestinal dysfunction after 4 weeks of intervention with compound probiotics.

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • Probiotic group

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators