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

NCT04133610 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1044

Last updated 2019-11-26

No results posted yet for this study

Summary

Comparison of the detection of human papillomavirus DNA in paired physician-obtained cervical swabs and self-sampled cervicovaginal swabs and evaluation of HPV prevalence in Czech women screening population.

Conditions

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.

Sponsors & Collaborators

  • National Institute for Cancer Research, Czech Republic

    collaborator OTHER

  • The Institute of Molecular and Translational Medicine, Czech Republic

    lead OTHER

Principal Investigators

  • Marian Hajduch, MD, PhD. · Palacky University in Olomouc, Faculty of Medicine and Dentistry

Study Design

Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
64 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-09-01
Primary Completion
2019-10-30
Completion
2019-11-25

Countries

  • Czechia

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04133610 on ClinicalTrials.gov