Exploring the Potential Benefits of Probiotic Yogurt

Last updated: March 2, 2025
Sponsor: Wecare Probiotics Co., Ltd.
Overall Status: Active - Recruiting

Phase

N/A

Condition

Constipation

Treatment

Yogurt control group

Probiotic yogurt group

Clinical Study ID

NCT06847919
WK20250207
  • Ages 18-65
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

This study aims to evaluate the effect of a high-activity probiotic yogurt on improving symptoms of chronic constipation, observing its regulatory effects on the gut microbiota and the incidence of adverse reactions in study participants over a 21-day intervention period.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Meet the Rome IV diagnosis criteria for chronic constipation;

  2. Patients who are able to understand clinical studies and are committed to complyingwith study requirements and procedures;

  3. Age 18-65. -

Exclusion

Exclusion Criteria:

  1. Systemic (diabetes, autoimmune diseases, cancer), gastrointestinal or liver diseasesknown to be associated with alterations in the gut microbiota;

  2. Patients who are pregnant or lactating;

  3. have taken antimicrobials, probiotics, or drugs that inhibit stomach acid orgastrointestinal motility in the past 6 weeks;

  4. Patients who changed their diet type during the study;

  5. Patients who are allergic or intolerant to any component of the investigationalproduct formulation;

  6. Patients with cardiovascular, cerebrovascular, liver, kidney and hematopoieticsystem and other serious diseases and endocrine diseases, mental patients;

  7. Stop taking the tested sample or add other drugs in the middle, unable to judge theefficacy or incomplete data;

  8. short-term use of objects related to the function of the test, affecting thejudgment of the result;

  9. have been dieting, exercising excessively, taking weight loss medications or takingmedications that may affect appetite in the past 3 months;

  10. Current or past excessive use of alcohol, drugs, or supplements that may causeintestinal dysfunction or interfere with the evaluation of the efficacy of the studyproduct -

Study Design

Total Participants: 84
Treatment Group(s): 2
Primary Treatment: Yogurt control group
Phase:
Study Start date:
February 25, 2025
Estimated Completion Date:
December 30, 2025

Connect with a study center

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

    Suzhou, Jiangsu 215200
    China

    Active - Recruiting

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