Clinical Trials Directory

Trials / Completed

CompletedNCT05900752

A Multi-Strain Probiotic Reduces the Frequency of Diarrhea in IBS-D Patients

A Multi-Strain Probiotic Reduces the Frequency of Diarrhea in IBS-D Patients: A Two-Center, Randomized, Double-Blind, Placebo-controlled Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
140 (actual)
Sponsor
Shenzhen Precision Health Food Technology Co. Ltd., · Other Government
Sex
All
Age
25 Years – 35 Years
Healthy volunteers
Accepted

Summary

The goal of this interventional clinical study is to study whether the consumption of QiMeiYan Probiotics in 25-35 young people with Mild irritable bowel syndrome (IBS Score 75 - 175) will reduce the frequency of Diarrhea. 140 eligible participants (70 males and 70 females) will be enrolled in two study sites and randomly assigned to two groups of products QiMeiYan Probiotics and placebo. All participants will consume assigned products once a day after meals and record the critical data such as photo of feces. Three site visits will be arranged and all clinical data will be captured and recorded into CTMS (Clinical Trial Management System) for statistical analysis. Researchers will compare the two groups to validate if the daily consumption of QiMeiYan Probiotics will reduce the frequency of Diarrhea in the study population.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTQiMeiYan Probioticsconsume one sachet of the assigned product, once a day after meals.
DIETARY_SUPPLEMENTPlacebo productconsume one sachet of the assigned product, once a day after meals.

Timeline

Start date
2023-06-19
Primary completion
2023-07-16
Completion
2023-07-16
First posted
2023-06-13
Last updated
2023-11-24

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05900752. Inclusion in this directory is not an endorsement.