Recruitment

Recruitment Status
Active, not recruiting

Inclusion Criteria

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)
Resident of the regions chosen for the study

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

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)
Resident of the regions chosen for the study

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