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Clinical Trial Summary

Women accessing the HPV-based screening programme for primary screening, will undergo cervical sampling and clinical data recording. Samples from high-risk HPV positive women (around 2000 expected) will be aliquoted for testing with new HPV molecular test, that will allow full genotyping and viral load quantification.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05193669
Study type Observational
Source Hiantis Srl
Contact
Status Active, not recruiting
Phase
Start date April 14, 2021
Completion date November 30, 2023

See also
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