Human Papillomavirus Self-sampling for Enhancing Cervical Screening During the War in Ukraine
Recruiting
N/A
Interventional Study
Cervical Cancer
Cervical Cancer Screening
Human Papillomavirus (HPV) Infection
Cervical Intraepithelial Neoplasia
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 – 60
- Sex
- Female
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 1,000 (estimated)
- Sponsor
- Karolinska Institutet · Other
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About This Trial
In 2020, a cervical screening center was established in Zaporizhzhia (Ukraine), initiating a pilot project to evaluate the prevalence of HPV among women in Eastern Ukraine. The findings were intended to lay the groundwork for the Ukrainian Ministry of Health in establishing a structured national screening program. However, all efforts were halted due to the nearby armed conflict, situated just 40 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female aged 30-60 years
* Intact uterus (no prior hysterectomy)
* Eligible for cervical cancer screening according to local guidelines
* Able to provide informed consent
* Able to perform self-sampling at home or at a clinic
Exclusion Criteria:
* History of total hysterectom…
Contacts