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The Prospective Cohort Study to Evaluate the Preventive Efficacy of HPV Vaccine in Japanese Women Aged 27-45 Years

A Nonrandomized, Non-double Blinded Prospective Cohort Study to Evaluate the Preventive Efficacy of Quadrivalent HPV6/11/16/18 Vaccine for the Persistent Infection of HPV16 Genotype or HPV18 Genotype in Japanese Women Aged 27-45 Years.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04022148
Enrollment
2800
Registered
2019-07-16
Start date
2019-08-01
Completion date
2020-12-31
Last updated
2019-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer of Cervix, Vaccinia

Keywords

uterine cervical cancer, HPV vaccine, cancer screening

Brief summary

A nonrandomized, non-double blinded prospective cohort study to evaluate the preventive efficacy of quadrivalent HPV6/11/16/18 vaccine for the persistent infection of HPV16 genotype or HPV18 genotype in Japanese women aged 27-45 years.

Detailed description

A series of evidence for HPV vaccines has demonstrated the efficacy in young women (Aged less than 26) across the globe. In contrast, limited evidence are available for the efficacy of the quadrivalent HPV6/11/16/18 vaccine in adult women (Aged 27+). Most importantly, evidence for Japanese adult women is not available to date. Nevertheless, , we hypothesize that the quadrivalent HPV6/11/16/18 vaccine demonstrate the efficacy also in Japanese adult women. The outcome from this trial will be the first local evidence, which brings a considerable impact in OB/GY academia where local evidence is weighed heavily compared with global evidence - serves as a strong basis to support catch up program of HPV vaccines for young adults. As a consequence, we believe this study will develop a local supportive evidence for prevention of HPV infection by an HPV vaccine in young adults, which results in substantial public health improvement through prevention of HPV infection in Japan where active recommendation is halted long time.

Interventions

BIOLOGICALGardasil

Experimental arm: Vaccine group VS Control arm: Non-Vaccine group

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
University of Fukui
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
27 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Women with normal cytology results confirmed in cervical cancer screening programs from May 2019 to March 2020 * 27-45 years-old * Intact uterus * Willing to undergo the HPV-DNA test (cobas4800) within 12 months

Exclusion criteria

* Pregnant women * Undergo treatment or the follow-up evaluation for CIN within the previous 12 months * Previously administered HPV vaccine

Design outcomes

Primary

MeasureTime frameDescription
The rate of the persistent infection48monthsPersistent infection is the cases that the cells from women with HPV16/18 genotype overexpressed p16 and Ki67.

Contacts

Primary ContactTetsuji Kurokawa, AP
kurotetu@u-fukui.ac.jp+81-776-61-8392
Backup ContactYoko Chino, A
yoyoyo@u-fukui.ac.jp+81-776-61-8392

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026