A Study on Immunity Duration Against Polio Over 18 Months Infants After 2 or 3 Primary Doses Sabin IPV in China
NCT ID: NCT04614597
Last Updated: 2022-03-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
774 participants
OBSERVATIONAL
2020-10-29
2021-12-21
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
A Study of Immunogenicity and Seroconversion With Sabin IPV Schedules in China.
NCT03597919
Sero-conversion Study for a Two-dose Schedule of Sabin IPV in China
NCT03546634
Immunogenicity and Safety Evaluation of Different Sequential Immunization Strategies by Sabin IPV and bOPV in Chinese Infants
NCT03147560
Assessing Immunogenicity of Intramuscular Sabin Inactivated Poliovirus Vaccine and Non-inferiority of Intradermal Fractional Inactivated Poliovirus Vaccine
NCT05460377
A Safety Study of Sabin Inactivated Poliovirus Vaccine in Infants
NCT05432141
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Since there is no any data about the protection duration of two-dose Sabin IPV schedules, China CDC propose to follow up the study cohort when all subjects are at least 18 months old to monitor persistence of antibody. So that, if the antibody levels are not high enough to protect children from the disease, remedial measures can be taken as soon as possible.So China CDC conduct this follow up study ,to
1. Evaluate the proportion of seroprotection of antibody against poliovirus at over 18 months of age infants after a 2-dose or a 3-dose primary schedule of Sabin IPV in Chinese children.
2. Measure neutralizing antibody titers against poliovirus type I, II and III at over 18 months of age infants after 2-dose Sabin IPV schedule, compared with 3-dose Sabin IPV schedule.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Three-dose schedule for Sabin IPV
Subjects already vaccinated Sabin IPV at 2, 3, and 4 months of age, collected two blood samples and laboratory test results were available.
Sabin strain inactivated polio vaccine
Sabin IPVs have been given to participants in previously study, blood specimens will be collected once all the subjects reach the age of 18months.
Two-dose schedule for Sabin IPV
Subjects already vaccinated Sabin IPV at 4 and 8-11 months of age, collected two blood samples and laboratory test results were available.
Sabin strain inactivated polio vaccine
Sabin IPVs have been given to participants in previously study, blood specimens will be collected once all the subjects reach the age of 18months.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Sabin strain inactivated polio vaccine
Sabin IPVs have been given to participants in previously study, blood specimens will be collected once all the subjects reach the age of 18months.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The subject was vaccinated either two doses or three doses Sabin IPV ,collected two blood samples and laboratory test results were available per protocol of pervious study
* The subject is at least 18 months age.
Exclusion Criteria
* The subject has received any polio vaccine product beyond the protocol of previous study.
18 Months
3 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
World Health Organization
OTHER
Shandong Province Centers for Disease Control and Prevention
OTHER
Centers for Disease Control and Prevention, China
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
AN Zhijie
Researcher of National Immunization Program
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Zijian Feng, MD
Role: STUDY_CHAIR
Centers for Disease Control and Prevention, China
Zhijie An, MPH
Role: PRINCIPAL_INVESTIGATOR
Centers for Disease Control and Prevention, China
Zundong Yin
Role: STUDY_DIRECTOR
Centers for Disease Control and Prevention, China
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Shandong Center for Disease Control and Prevention
Jinan, , China
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
201935
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.