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An Observational Study on the Impact of Nutritional Support on the Recurrence Rate of Acute Infectious Diarrhea in Children with Varying Nutritional Risks in a Real-World Clinical Setting

An Observational Study on the Impact of Nutritional Support on the Recurrence Rate of Acute Infectious Diarrhea in Children with Varying Nutritional Risks in a Real-World Clinical Setting

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097225
Enrollment
Unknown
Registered
2025-02-14
Start date
2025-03-05
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Acute infectious diarrhea in children

Interventions

Control:No additional nutritional products were provided during the recovery period from diarhoea
Nutritional Support:Probiotics were added for 1 month during the recovery period of diarrhea

Sponsors

Shandong Institute of Pharmaceutical Research Ethics Committee
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1.Enrollment age: 3-10 years old children, nutritional risk screening showed that there were different degrees of nutritional risk; 2.The patient was diagnosed with acute infectious diarrhea; 3.Informed consent: The children's guardians signed the informed consent and understood the content, purpose and risks of the study; 4.Parent participation: parents need to be able and committed to feedback their children's symptoms, health status, and nutritional intake data on time through a follow-up system (such as a mobile App or WeChat applet);

Exclusion criteria

Exclusion criteria: 1.Children allergic to zinc or probiotics; 2.Patients with severe malnutrition or other serious medical conditions requiring specific treatment; 3.Chronic diseases: such as serious medical diseases, metabolic disorders, immune system diseases, etc; 4.Patients who had received probiotic supplements within the last 3 months; 5.Patients who participated in other relevant studies within the last 3 months; 6.Patients who were deemed by the investigator to be ineligible to participate in the trial;

Design outcomes

Primary

MeasureTime frame
The recurrence rate of diarrhea& The rate of relief of symptoms;Duration of Diarrhea;

Secondary

MeasureTime frame
Nutritional status;Indicators of immunity;

Countries

China

Contacts

Public ContactLiuxiang Ye

Shandong Institute of Pharmaceutical Research Ethics Committee

ylx@yuangao.email+86 20 38019026

Outcome results

None listed

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