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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04170140
Other study ID # DNG00042
Secondary ID U1111-1233-9599
Status Completed
Phase
First received
Last updated
Start date January 7, 2020
Est. completion date March 5, 2020

Study information

Verified date April 2022
Source Sanofi
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

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.


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date March 5, 2020
Est. primary completion date March 5, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion criteria: - Healthcare professionals who are current or past prescribers of Dengvaxia Exclusion criteria: - Healthcare professionals who have never prescribed Dengvaxia - Healthcare professionals who may have a conflict of interest with the survey (i.e. Healthcare professionals employed by regulatory bodies, pharmaceutical industries) - Healthcare professionales who have participated in testing the questionnaire for comprehensibility, consistency and the appropriateness of medical terms The above information is not intended to contain all considerations relevant to participation in the survey.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention
Questionnaire

Locations

Country Name City State
France Real World Evidence Solutions IQVIA La Defense

Sponsors (1)

Lead Sponsor Collaborator
Sanofi Pasteur, a Sanofi Company

Country where clinical trial is conducted

France, 

References & Publications (1)

Almas MF, Toussi M, Valero E, Moureau A, Marcelon L. A cross-sectional survey to evaluate prescribers' knowledge and understanding of safety messages following Dengvaxia(R) product information update. Pharmacoepidemiol Drug Saf. 2022 Jul;31(7):758-768. do — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Healthcare professionals' knowledge and understanding of key safety messages provided in risk minimization measures materials Knowledge and understanding of key safety messages are assessed through a questionnaire Day 0
Secondary Healthcare professionals' knowledge of Dengvaxia product information Knowledge of Dengvaxia product information (age indication and contraindications) is assessed through a questionnaire Day 0
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