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.
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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

Laila Sara Arroyo Mühr, PhD

+46700917250

sara.arroyo.muhr@ki.se

CONTACT

Joakim Dillner, Professor

+46724682460

joakim.dillner@ki.se

CONTACT