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To investigate whether bifidobacterium brevis can improve infantile diarrhea through its influence on intestinal microbiota

To investigate whether bifidobacterium brevis can improve infantile diarrhea through its influence on intestinal microbiota

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099463
Enrollment
Unknown
Registered
2025-03-24
Start date
2024-01-26
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Infantile infectious diarrhea

Interventions

Control,C:None
Infantile diarrhea,ID:None
IDMPR:Receive conventional treatment with montmorillonite powder, along with oral probiotics
IDMPL:He received conventional treatment with montmorillonite powder and an oral placebo

Sponsors

The Second People's Hospital of Jingdezhen
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The clinical manifestations were abdominal distension, diarrhea, abdominal pain, increased frequency of stool, watery stool, loss of appetite, etc. 2. The onset time was more than 5 days, and there was no digestive ulcer or digestive system tumor after relevant examination. 3. No other drugs or probiotics were used in the first 3 months after the completion of treatment, and parents agreed to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. High fever persists, there is secondary diarrhea. 2. Have a recent history of antibiotic or antidiarrheal therapy, have a serious active viral or bacterial infection, and have not been controlled by treatment. 3.Have any other serious or chronic illness that the investigator believes may affect the patient's treatment, follow-up, or evaluation. It includes any uncontrolled and clinically significant neurological, psychiatric, immune-regulatory, metabolic and infectious diseases. 4. Patients who are not suitable for probiotic-assisted therapy after diagnosis and evaluation by clinicians.

Design outcomes

Primary

MeasureTime frame
Gut microbiota composition;Observation on the efficacy of diarrhea;Hart diarrhea scale;High-throughput sequencing of stool samples;Detection of the source of infection;

Secondary

MeasureTime frame
Clinical blood test;

Countries

China

Contacts

Public ContactHongying Yu

Jingdezhen Second People's Hospital

yyb89009@qq.com+86 139 7986 2619

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026