Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07081100

Probiotics and Non-Organic Gastrointestinal Improvement

Led by Wecare Probiotics Co., Ltd. · Updated on 2025-07-31

50

Participants Needed

1

Research Sites

29 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Probiotics and Non-Organic Gastrointestinal Improvement

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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.
Not Eligible

You will not qualify if you...

  • Use of drugs affecting intestinal flora (antibiotics, probiotics, intestinal mucosal protectants, herbal medicines, etc.) for more than 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.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Suzhou Ninth People's Hospital Suzhou Ninth Hospital affiliated to Soochow University

Suzhou, Jiangsu, China, 215200

Actively Recruiting

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Research Team

Y

Ying Jin, Doctor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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