About this trial
Chinese survey data indicate that the incidence rate of diarrhea in the general population ranges from 0.17 to 0.70 episodes per person-year, whereas among children under five years of age, the rate is significantly higher, ranging from 2.50 to 3.38 episodes per person-year. Over recent decades, rapid economic development has contributed substantially to the reduction of mortality associated with infectious diseases. However, emerging challenges-such as increasing antimicrobial resistance and heightened population mobility-have complicated efforts in infectious disease prevention and control. In a phase III clinical trial of the recombinant B subunit/bacterial whole-cell cholera vaccine (enteric-coated capsule), a statistically significant difference was observed in the overall incidence of diarrhea between the vaccinated group (12.9%) and the control group (26.7%) (P \< 0.01). Findings from similar vaccine studies conducted in Sweden have demonstrated cross-protection against diarrhea caused by enterotoxigenic Escherichia coli (ETEC) and other intestinal pathogens. Specifically, the vaccine conferred a 50% protection rate against Salmonella enterica infections, 82% against mixed infections involving ETEC and Salmonella, and 71% against mixed infections involving ETEC and other pathogens. Evidence from relevant studies suggests that the recombinant B subunit/bacterial whole-cell cholera vaccine may offer protective benefits against non-cholera infectious diarrhea. Nevertheless, there remains a paucity of real-world effectiveness data, particularly in pediatric populations who bear a disproportionately high burden of diarrheal disease.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age ≥ 2 years old, ≤ 14 years old, male or female.
Not vaccinated against cholera.
Obtain the consent of the study subject or guardian and sign the informed consent form.
The subjects and their guardians were able to comply with the requirements of the clinical study protocol.
Disqualifiers
Exclusion Criteria for First Inoculation:
Patients with febrile illness (axillary temperature ≥ 37.0 °C on the day of vaccination), other acute diseases, and diarrhea within 7 days before vaccination.
Use of antibiotics within 7 days prior to vaccination.
Patients with gastric ulcer, abnormal gastric acid secretion and other gastric diseases or discomfort.
Trial design
Parallel
Treatments tested in this trial
Recombinant subunit B/bacterial cholera vaccine (enteric-coated capsules)
Biological/VaccineThe participants in the experimental group will be given three oral doses of recombinant subunit B/bacterial cholera vaccine (enteric-coated capsules) on D0, D7, and D28 .
Placebo
Biological/VaccineThe participants in the Control group will be given three oral doses of recombinant subunit B/bacterial cholera vaccine (enteric-coated capsules) Placebo on D0, D7, and D28 .
Treatment groups
Trial outcomes
Primary outcomes
the incidence of infectious diarrhea in the vaccinated group and placebo group
Protective effect of recombinant subunit B/bacterial cholera vaccine (enteric-coated capsules) against infectious diarrhea due to enteropathogens (except Vibrio cholerae) (Day 7 after full immunization to the end of the study).
Sponsors and contacts
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