Gastrointestinal Function
Conditions
Brief summary
To verify the improvement of gastrointestinal function in patients with non-organic gastrointestinal dysfunction after 4 weeks of intervention with compound probiotics.
Interventions
Participants took a freeze-dried probiotic powder every day, half an hour after a meal.
Sponsors
Study design
Eligibility
Inclusion criteria
* 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 criteria
* 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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improvement of gastrointestinal function in study participants | 4 weeks | The severity of gastrointestinal symptoms was assessed by the Gastrointestinal Symptom Rating Scale (GSRS). Each item is scored from 1 (no symptoms) to 7 (extremely severe symptoms. Higher scores indicate worse gastrointestinal dysfunction. |
Countries
China