A Multicenter Cohort Study Assessing the Efficacy and Adverse Effects of HPV Vaccination in Chinese Women

Sponsor
Fujian Maternity and Child Health Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05932576
Collaborator
(none)
12,000
5
25
2400
96

Study Details

Study Description

Brief Summary

Human papillomavirus (HPV) is currently one of the most common sexually transmitted infections, according to its carcinogenicity is divided into high-risk genotypes and low-risk genotypes, research has confirmed that carcinogenic HPV type continuous infection leads to a higher incidence of condyloma acuminatum and cervical cancer, while increasing the oropharyngeal cancer, vaginal cancer and other related cancer risk. HPV vaccines have been widely introduced worldwide to prevent cancers of the lower genital tract such as cervical, anal and vulvar cancers. For different types of HPV vaccine, divided into domestic bivalent, imported bivalent (GlaxoSmithKline), quadrivalent (Merck) and nine-valent (Merck) HPV vaccine, four vaccines all prevent HPV 16/18 high-risk type infection disease, and the four and nine-valent HPV vaccine prevention genotypes are different, and different price number of protection rates, vaccination objects and immunization procedures are slightly different. At the same time, studies have shown that women after HPV vaccine, arm redness, swelling, heat and pain have a high incidence of adverse reactions, often accompanied by menstrual disorders, sleep problems, emotional irritability, fever, dizziness, headache and other adverse reactions risk, so we plan to design a multicenter cohort study to evaluate the effectiveness of HPV vaccine with different prices. At the same time, the adverse reaction symptoms of HPV vaccine in the female population of appropriate age were monitored.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study was led by the Fujian Provincial Maternal and Child Health Hospital, with the following research centers: Xiangya Hospital of Central South University, Fujian Provincial Center for Disease Control and Prevention, Shenzhen Maternal and Child Health Hospital, Hubei Provincial Maternal and Child Health Hospital, Shandong Province and Shaanxi Province. Recruitment was conducted in 6 provinces in different regions of China, and 2000 subjects were recruited in each province. A total of 12,000 subjects were recruited. Each subject was evaluated within 3 to 12 months after the last dose of HPV vaccine, and adverse reaction symptoms were queried by telephone follow-up and face-to-face. Peripheral blood 1 tube (3ml) was collected to detect the concentration of comprehensive antibodies to HPV vaccine. A multicenter cohort study was conducted to evaluate the effectiveness of HPV vaccine and to monitor the symptoms of adverse reactions to HPV vaccine in the female population of appropriate age.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    12000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    A Multicenter Cohort Study Assessing the Efficacy and Adverse Effects of Different HPV Vaccination in Chinese Women
    Actual Study Start Date :
    Dec 1, 2022
    Anticipated Primary Completion Date :
    Dec 31, 2024
    Anticipated Study Completion Date :
    Dec 31, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    The HPV vaccine group

    Women aged 9-45 years who received the last dose of HPV vaccine within the past 12 months were included, and each subject was evaluated within 3-12 months after the last dose of HPV vaccine. Adverse reaction symptoms were queried by telephone follow-up and face-to-face, and peripheral blood tube (3ml) was collected to detect the concentration of comprehensive antibody to HPV vaccine.

    Outcome Measures

    Primary Outcome Measures

    1. HPV vaccine neutralizing antibody detection [Within 3 to 12 months of each subject's last dose of HPV vaccine]

      All participants were tested for neutralizing antibodies to the HPV vaccine

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    9 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Female, aged 9-45; Get the last dose of HPV vaccine within 12 months.
    Exclusion Criteria:
    • Pregnancy or lactation during HPV vaccination; Those who refuse follow-up and informed consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Fujian Maternity and Child Health Hospital Fuzhou Fujian China 350001
    2 Fujian Provincial Center for Disease Control and Prevention Fuzhou Fujian China
    3 Maternal and Child Health Hospital of Shenzhen Province Shenzhen Guangdong China
    4 Maternal and Child Health Hospital of Hubei Province Wuhan Hubei China
    5 Xiangya Hospital, Central South University Changsha Hunan China

    Sponsors and Collaborators

    • Fujian Maternity and Child Health Hospital

    Investigators

    • Study Chair: Sun Pengming, PhD, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Binhua Dong, Laboratory of Gynecologic Oncology, Fujian Maternity and Child Health Hospital
    ClinicalTrials.gov Identifier:
    NCT05932576
    Other Study ID Numbers:
    • HVAC2302
    First Posted:
    Jul 6, 2023
    Last Update Posted:
    Jul 6, 2023
    Last Verified:
    Jun 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Jul 6, 2023