Recruiting NCT07081100
Probiotics and Non-Organic Gastrointestinal Improvement
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Probiotic group.
- Who it may be relevant to
- Registry conditions: Gastrointestinal Function. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Study on the Effect of Probiotics on Improving Gastrointestinal Function in Patients With Non-organic Gastrointestinal Dysfunction
Overview
To verify the improvement of gastrointestinal function in patients with non-organic gastrointestinal dysfunction after 4 weeks of intervention with compound probiotics.
Interventions
- Dietary supplement Probiotic group
Participants took a freeze-dried probiotic powder every day, half an hour after a meal.
Primary outcome measures
- Improvement of gastrointestinal function in study participants [Time frame: 4 weeks]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
China · 1 center
- Suzhou Ninth People's Hospital Suzhou Ninth Hospital affiliated to Soochow University — Suzhou
Identifiers
NCT: NCT07081100 · WK20250716