Concomitant HPV Vaccination and HPV Screening HPV Infection and Cervical Cancer in Sweden

Recruiting Phase 4 Interventional Study
HPV Infection CIN 2/3 Cervical Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
22 – 27
Sex
Female
Trial phase
Phase 4
Study type
Interventional
Purpose
Prevention
Participants needed
150,000 (estimated)
Sponsor
Miriam Elfström · Government
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About This Trial

The study aims to evaluate whether organised, concomitant HPV vaccination and HPV screening offered to all resident women aged 22-27 will result in a more rapid elimination of HPV infection in Sweden. This objective will be examined at the population level.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Eligible women will include resident women within the age range of 22-26, who have not opted out of the screening program and who consent to participate in the study. Women who respond to the invitation and attend screening will be screened with HPV testing by the current rou…
Contacts

Miriam Elfström, PhD

+46703816277

miriam.elfstrom@sll.se

CONTACT

Helena Andersson, PhD

+46768871126

helena.t.andersson@sll.se

CONTACT