RecruitingNCT06253169

HPV DNA Self-sampling in a General Practitioner's Office.

Benefit of Self-sampling for HPV DNA in a General Practitioner's Office to Improve Participation in Cervical Screening - The ASTRA Study.


Sponsor

Patient Organization Veronica

Enrollment

2,000 participants

Start Date

Mar 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

One of the limitations of organized cervical screening in the Czech Republic is the lack of participation in preventive gynecological examinations. The aim of the project is to evaluate the benefits of self-sampling for HPV DNA in general practitioners' outpatient clinics to improve population participation in cervical screening.


Eligibility

Sex: FEMALEMin Age: 30 Years

Inclusion Criteria3

  • Signed informed consent for statistical data processing and consent to the processing of personal data
  • Age 30+
  • HPV test never performed or performed more than 3 years ago or patient does not know

Exclusion Criteria6

  • Refusal to participate
  • Pregnancy and puerperium
  • Menses
  • History of hysterectomy
  • HPV test performed \<3 years ago with negative result
  • Regular participation in screening and concurrent age 35, 45 or 55 years (test will be performed in the same year of screening).

Interventions

DIAGNOSTIC_TESTHPV DNA self-test

HPV DNA swab from the cervix performed by the patient herself.


Locations(2)

CGOP, s.r.o.

Prague, Czechia

Department of Gynecology, Obstetrics and Neonatology, General University Hospital, First Faculty of Medicine, Charles University

Prague, Czechia

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06253169


Related Trials