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Clinical Trial Summary

The aim of the study is to develop robust analytical protocols for first-void urine sample preparation and antibody assays to monitor natural and/or vaccine induced immunity against HPV (Human Papillomavirus).


Clinical Trial Description

In total 57 women will be included in this trial: 38 vaccinated with an prophylactic HPV vaccine and 19 not vaccinated with a prophylactic HPV vaccine. These women are asked to collect a first-void urine sample with the Colli-PeeTM device (Novosanis). Hereafter, a blood sample of 5-10 cc is collected. The collected urine and blood samples will be used for the development and optimisation of robust analytical protocols for sample preparation and antibody assays. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02714114
Study type Observational
Source Universiteit Antwerpen
Contact
Status Completed
Phase N/A
Start date September 2015
Completion date December 2015

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