NCT04133610View on ClinicalTrials.gov

HPVPro Study: Comparison of HPV Detection in Clinician-collected Cervical Swabs and Self-sampled Cervicovaginal Swabs

NACompletedINTERVENTIONAL
Enrollment

1,044

Participants

Timeline

Start Date

September 1, 2018

Primary Completion Date

October 30, 2019

Study Completion Date

November 25, 2019

Conditions
Cervical CancerCervical DysplasiaHuman Papillomavirus Infection
Interventions
DIAGNOSTIC_TEST

Self-sampling using digene HC2 DNA Collection Device

All women will undergo a clinician-collected cervical swab and self-collected cervicovaginal swab.

DIAGNOSTIC_TEST

Self-sampling using Evalyn Brush

All women will undergo a clinician-collected cervical swab and self-collected cervicovaginal swab.

Trial Locations (3)

Unknown

GYN-PREN, Ltd., Frýdek-Místek

GYNPRENATAL, Ltd., Havířov

MEDIOL, Ltd., Olomouc

All Listed Sponsors
collaborator

National Institute for Cancer Research, Czech Republic

OTHER

lead

The Institute of Molecular and Translational Medicine, Czech Republic

OTHER

NCT04133610 - HPVPro Study: Comparison of HPV Detection in Clinician-collected Cervical Swabs and Self-sampled Cervicovaginal Swabs | Biotech Hunter | Biotech Hunter