Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
Healthy Volunteers
NCT07033091

Prevalence of Human Papillomavirus (HPV) in a Healthy Population: A Feasibility Study of Oropharyngeal Cancer Screening

Led by The Institute of Molecular and Translational Medicine, Czech Republic · Updated on 2026-02-13

20000

Participants Needed

5

Research Sites

304 weeks

Total Duration

On this page

Sponsors

T

The Institute of Molecular and Translational Medicine, Czech Republic

Lead Sponsor

N

National Institute for Cancer Research, Czech Republic

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study defines the prevalence of oral infection with high-risk human papillomaviruses (hrHPV) in individuals over 40 years of age in the Czech Republic. It also establishes an effective methodology for oropharyngeal carcinoma screening and optimization of screening and testing procedures.

CONDITIONS

Official Title

Prevalence of Human Papillomavirus (HPV) in a Healthy Population: A Feasibility Study of Oropharyngeal Cancer Screening

Who Can Participate

Age: 40Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants aged 40 years or older at the time of enrollment.
  • Individuals who are capable of rinsing the oral cavity by gargling independently.
  • Signed informed consent for study participation, molecular-genetic testing, and personal data processing.
Not Eligible

You will not qualify if you...

  • Previously diagnosed head and neck cancer.

AI-Screening

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Trial Site Locations

Total: 5 locations

1

Masaryk Memorial Cancer Institute

Brno, Czechia

Not Yet Recruiting

2

Stomatologická klinika, Fakultní nemocnice u sv. Anny

Brno, Czechia

Actively Recruiting

3

Stomatologické centrum ARTDENT s.r.o.

Jihlava, Czechia, 586 01

Actively Recruiting

4

Klinika zubního lékařství Fakultní nemocnice Olomouc

Olomouc, Czechia, 77900

Actively Recruiting

5

CLINIQ Dejvice

Prague, Czechia, 160 00

Actively Recruiting

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Research Team

V

Vladimira Koudelakova, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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