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Clinical Trial Summary

The investigators would remind the guardians of observation after immunization via sending short message and collect the information of AEFI by two ways, short message/telephone and website questionnaire.


Clinical Trial Description

The investigators will compare the rate between active and inactive surveillance of AEFI ;


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01830257
Study type Interventional
Source Beijing Center for Disease Control and Prevention
Contact
Status Enrolling by invitation
Phase Phase 4
Start date April 2013
Completion date June 2014

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