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Clinical Trial Summary

The aim of this study is to assess efficacy of the screening with concurrent liquid-based cytology and HPV DNA testing for the primary cervical cancer screening over 7 years.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01895517
Study type Interventional
Source Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan
Contact
Status Completed
Phase Phase 4
Start date June 7, 2013
Completion date May 31, 2023

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