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The Epidemiologic Study of Human Papillomavirus Infection and Related Diseases

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ClinicalTrials.gov Identifier: NCT02188004
Recruitment Status : Completed
First Posted : July 11, 2014
Last Update Posted : May 7, 2019
Sponsor:
Collaborator:
Liuzhou center of disease prevention and control
Information provided by (Responsible Party):
Jun Zhang, Xiamen University

Brief Summary:

primary purpose:Evaluate the prevalence and incidence of HPV infection and related diseases in subjects.

Secondary purpose:Analyze risk factors of HPV infection and related diseases.


Condition or disease
Human Papillomavirus Infection Genital Warts

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Study Type : Observational
Actual Enrollment : 4691 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: The Epidemiologic Study of Human Papillomavirus Infection and Related Diseases In Male and Female Aged Over 18 Years In China
Study Start Date : June 2014
Actual Primary Completion Date : May 2016
Actual Study Completion Date : May 2016



Primary Outcome Measures :
  1. prevalence and incidence of HPV infection [ Time Frame: 1 year ]
    Evaluate the prevalence and incidence of HPV infection and related diseases in subjects


Secondary Outcome Measures :
  1. risk factors of HPV infection and related diseases [ Time Frame: 1 year ]
    Analyze risk factors of HPV infection and related diseases.


Biospecimen Retention:   Samples With DNA

Male:Two swabs were used to collect exfoliated skin cells from the coronal sulcus /glans/shaft and anal

Female:Three swabs were used to collect exfoliated skin cells from the vagina,vulva and anal



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
5000 healthy volunteers will be recruited from the residents of Liuzhou through advertisment.
Criteria

Inclusion Criteria:

  • ages 18 to 55 years;
  • residents of the study site;
  • at least one sex partner;
  • Be able to understand and comply with the request of the protocol.

Exclusion Criteria:

  • pregnant;
  • has received HPV vaccines.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02188004


Locations
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China, Guangxi
Liuzhou Center of disease prevention and control
Liuzhou, Guangxi, China
Sponsors and Collaborators
Jun Zhang
Liuzhou center of disease prevention and control
Investigators
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Study Chair: Jun Zhang Xiamen University
Principal Investigator: Ming-Qiang Li Liuzhou center of disease prevention and control
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Jun Zhang, professor, Xiamen University
ClinicalTrials.gov Identifier: NCT02188004    
Other Study ID Numbers: HPV-EPI-001
First Posted: July 11, 2014    Key Record Dates
Last Update Posted: May 7, 2019
Last Verified: May 2019
Keywords provided by Jun Zhang, Xiamen University:
HPV
genital warts
Additional relevant MeSH terms:
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Infection
Communicable Diseases
Papillomavirus Infections
Condylomata Acuminata
DNA Virus Infections
Virus Diseases
Tumor Virus Infections
Warts
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Skin Diseases, Viral
Skin Diseases, Infectious
Skin Diseases