Self-sampling for Non-attenders to Cervical Cancer Screening
Recruiting
N/A
Interventional Study
Cervical Cancer
Cervical Dysplasia
Human Papillomavirus Infection
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 30 – 65
- Sex
- Female
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 15,000 (estimated)
- Sponsor
- The Institute of Molecular and Translational Medicine, Czech Republic · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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.
* Wo…
Contacts