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Probiotics and Non-Organic Gastrointestinal Improvement

Study on the Effect of Probiotics on Improving Gastrointestinal Function in Patients With Non-organic Gastrointestinal Dysfunction

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07081100
Enrollment
50
Registered
2025-07-23
Start date
2025-08-05
Completion date
2026-03-01
Last updated
2025-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal Function

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

DIETARY_SUPPLEMENTProbiotic group

Participants took a freeze-dried probiotic powder every day, half an hour after a meal.

Sponsors

Wecare Probiotics Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

MeasureTime frameDescription
Improvement of gastrointestinal function in study participants4 weeksThe 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

Contacts

Primary ContactYing Jin, Doctor
sunny13211@sina.com13375163966

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026