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Study on immune persistence of group A and Group C encephalitis conjugate vaccine and immunogenicity of different encephalitis vaccine after enhanced immunization

Study on immune persistence of group A and Group C encephalitis conjugate vaccine and immunogenicity of different encephalitis vaccine after enhanced immunization

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113915
Enrollment
Unknown
Registered
2025-12-04
Start date
2024-08-14
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Epidemic cerebrospinal meningitis

Interventions

Intervention Group 1:Receive the ACYW group quadrivalent meningococcal conjugate vaccine.
Intervention Group 2:Receive the AC group bivalent meningococcal conjugate vaccine.
Control group:Receive the bivalent meningococcal polysaccharide vaccine of the AC group under the National Immunization Program.

Sponsors

Immunization Program Center, Chinese Center for Disease Control and Prevention
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 4 Years

Inclusion criteria

Inclusion criteria: 1.Children aged 3 and above but under 4 years old; 2. Have received two doses of MPCV-AC within 12 months of age; 3. Has not received any third dose of meningococcal vaccine; 4. The guardians of the children give informed consent and participate voluntarily.

Exclusion criteria

Exclusion criteria: 1. Have a history of chronic diseases (such as immune system dysfunction, kidney disease, neurological disorders, metabolic diseases, etc.); 2. Suffering from congenital diseases, such as congenital heart disease, congenital immune deficiency, etc. 3. Have received immunoglobulin or blood product treatment within the three months prior to the study; 4. Have a history of meningococcal meningitis; 5. At the time of investigation, the individual suffered from moderate to severe acute diseases, infections or febrile diseases (axillary temperature >37.3?); 6. There are contraindications to vaccination.

Design outcomes

Primary

MeasureTime frame
Bactericidal Antibody Titers against neisseria meningitidis of Serogroup A;Bactericidal Antibody Titers against neisseria meningitidis of Serogroup C;Serum IgG antibody concentration of Neisseria meningitidis group A;Serum IgG antibody concentration of Neisseria meningitidis group C;

Secondary

MeasureTime frame
Interleukin-2;Interleukin-7;Interferon-?;

Countries

China

Contacts

Public ContactZheng Hui

Immunization Program Center, Chinese Center for Disease Control and Prevention

zhenghui@chinacdc.cn+86 83159521

Outcome results

None listed

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