Status:

UNKNOWN

Explore Active Surveillance Mode of the Community's Adverse Event Following Immunization(AEFI)

Lead Sponsor:

Beijing Center for Disease Control and Prevention

Conditions:

Adverse Reaction to Drug

Eligibility:

All Genders

Phase:

PHASE4

Brief 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 questionna...

Detailed Description

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

Eligibility Criteria

Inclusion

  • According with the regular vaccination
  • Immunization the acellular pertussis diphtheria tetanus vaccine and Measles and rubella combined vaccine

Exclusion

  • Disapproval the AEFI information

Key Trial Info

Start Date :

April 1 2013

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 1 2014

Estimated Enrollment :

1000 Patients enrolled

Trial Details

Trial ID

NCT01830257

Start Date

April 1 2013

End Date

June 1 2014

Last Update

April 12 2013

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