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Intervention study on the adjuvant effect of probiotic solid drink (Bifidobacterium lactis XLTG11) on the treatment of acute watery diarrhea in children

To evaluate the clinical efficacy and safety of bifidobacterium animalis strain XLTG11 in improving acute watery diarrhea in children

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055283
Enrollment
Unknown
Registered
2022-01-05
Start date
2022-12-31
Completion date
Unknown
Last updated
2023-01-23

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

Conditions

dysentery

Interventions

intervention group:Conventional treatment + probiotic solid drink (Bifidobacterium lactis XLTG11)
control group:Conventional treatment

Sponsors

Chengdu Women and Children's Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 3 Years

Inclusion criteria

Inclusion criteria: 1. Aged 0-3 years; 2. Diarrhea lasts for more than 12 hours but less than 72 hours; 3. Judged as non-bacterial infectious diarrhea; 4. Clinically mild to moderate dehydration.

Exclusion criteria

Exclusion criteria: 1. Chronic and persistent diarrhea; 2. Outlet obstruction caused by congenital intestinal malformation and difficulty in defecation; 3. Nervous system developmental abnormalities and severe organic diseases, severe malnutrition, immunodeficiency diseases, pancreatic dysfunction, pus and bloody stools, short bowel syndrome, bile or bloody vomit; 4. Secondary diarrhea; 5. Severe dehydration and serious condition need to be admitted to PICU for treatment; 6. Have taken probiotics before or within one month of the treatment for this disease; 7. Antibiotics are expected to be used to treat children during the trial; 8. Allergic diarrhea.

Design outcomes

Primary

MeasureTime frame
Number of diarrhea;Stool property;

Countries

China

Contacts

Public ContactChen Ke

Chengdu Women and Children's Central Hospital

263662086@qq.com+86 13981782973

Outcome results

None listed

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