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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02188004
Other study ID # HPV-EPI-001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2014
Est. completion date May 2016

Study information

Verified date May 2019
Source Xiamen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 4691
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility 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.

Study Design


Locations

Country Name City State
China Liuzhou Center of disease prevention and control Liuzhou Guangxi

Sponsors (2)

Lead Sponsor Collaborator
Jun Zhang Liuzhou center of disease prevention and control

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary prevalence and incidence of HPV infection Evaluate the prevalence and incidence of HPV infection and related diseases in subjects 1 year
Secondary risk factors of HPV infection and related diseases Analyze risk factors of HPV infection and related diseases. 1 year
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