Recruitment

Recruitment Status
Active, not recruiting

Inclusion Criteria

Resident of the regions chosen for the study
Having received two doses of Gardasil in 2008-2009, 2009-2010,2010-2011 or 2011-2012 according to 0, 6 months Schedule (between 4 and 12 months)
Resident of the regions chosen for the study
Having received two doses of Gardasil in 2008-2009, 2009-2010,2010-2011 or 2011-2012 according to 0, 6 months Schedule (between 4 and 12 months)

Exclusion Criteria

Being considered immunosuppressed at time of vaccination (9-10 years-old) or at recruitment visit
Being pregnant at recruitment visit
Being considered immunosuppressed at time of vaccination (9-10 years-old) or at recruitment visit
Being pregnant at recruitment visit

Summary

Conditions
Human Papillomavirus Infections
Type
Interventional
Phase
Phase 3
Design
  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Masking: Single (Outcomes Assessor)
  • Primary Purpose: Prevention

Participation Requirements

Age
Between 14 years and 16 years
Gender
Only females

Inclusion Criteria

Resident of the regions chosen for the study
Having received two doses of Gardasil in 2008-2009, 2009-2010,2010-2011 or 2011-2012 according to 0, 6 months Schedule (between 4 and 12 months)
Resident of the regions chosen for the study
Having received two doses of Gardasil in 2008-2009, 2009-2010,2010-2011 or 2011-2012 according to 0, 6 months Schedule (between 4 and 12 months)

Exclusion Criteria

Being considered immunosuppressed at time of vaccination (9-10 years-old) or at recruitment visit
Being pregnant at recruitment visit
Being considered immunosuppressed at time of vaccination (9-10 years-old) or at recruitment visit
Being pregnant at recruitment visit

Tracking Information

NCT #
NCT02009800
Collaborators
  • Centre hospitalier de l'Université de Montréal (CHUM)
  • Quebec Public Health National Institute
  • Ministere de la Sante et des Services Sociaux
  • Institut national de santé publique du Quebec
Investigators
Not Provided