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Clinical Trial Summary

The primary objective of the study is to evaluate the effectiveness of additional risk minimization measures material by assessing the knowledge and understanding of healthcare professionals regarding the key safety messages provided in the material. The secondary objective of the study is to evaluate if healthcare professionals know Dengvaxia product information, namely, age indication and contraindications.


Clinical Trial Description

The study is a cross-sectional Survey. Study data are collected through a questionnaire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04170140
Study type Observational
Source Sanofi
Contact
Status Completed
Phase
Start date January 7, 2020
Completion date March 5, 2020

See also
  Status Clinical Trial Phase
Recruiting NCT04486638 - Dengvaxia US Pregnancy Registry
Completed NCT04023708 - Observational Study to Evaluate the Safety of CYD Tetravalent Dengue Vaccine (CYD-TDV) in Pregnant Women and Their Offsprings Inadvertently Exposed During Pregnancy