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Clinical Trial Summary

This study is a cross-sectional study to evaluate accuracy of high-risk DNA-HPV testing using HPV Diagnostic Kit (Bio Farma) compared to Standard Kit (COBAS® 6800 HPV from Roche Molecular Systems) RT-PCR based in urine and cervical swab specimens.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06111911
Study type Interventional
Source PT Bio Farma
Contact
Status Completed
Phase N/A
Start date April 1, 2022
Completion date October 29, 2022

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