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Self-sampling kit for cervical cancer screening in women who do not attend screening

Tests a self-collected HPV swab for cervical cancer screening in women aged 30 to 65.

Plain-language title generated from the registry record
Registry title: Self-sampling for Non-attenders to Cervical Cancer Screening

Key facts

Where
Olomouc, CzechiaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 30 and 65 years old?

Source: NCT04226313, who can take part

Where in Czechia

  • University Hospital OlomoucOlomouc, CzechiaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
The Institute of Molecular and Translational Medicine, Czech Republic
Trial code
NCT04226313
Record updated
23 March 2026
Original description
The trial will evaluate whether self-sampling and human papillomavirus (HPV) testing may increase cervical cancer screening attendance among under-screened women in Czech Republic. Different ways of offering self-sampling device will be evaluated.Read full original descriptionShow less

Cervical Cancer Prevention Using Self-sampling and Human Papillomavirus Detection

The trial will evaluate whether self-sampling and human papillomavirus (HPV) testing may increase cervical cancer screening attendance among under-screened women in Czech Republic. Different ways of offering self-sampling device will be evaluated.

Inclusion: Women with age 30-65 years; for arm A women > 65 years are allowed; Women live in the Czech Republic; Women who have not participate in cervical cancer screening program in the Czech Republic for at least 3 years (Arm B and C); Women with completed informed consent; Women capable of self-sampling of cervicovaginal swab.

Exclusion: Pregnant women; Women with no sexual intercourse experience; Women after hysterectomy including cervix.

ClinicalTrials.gov NCT04226313