Clinical trial Recruiting at 1 site Interventional Ages Any age to 35 Women only

Examining HPV infections and vaccine attitudes among Slovenian women

Official title: Characteristics of Human Papillomavirus (HPV) Infections and HPV Vaccine Attitudes Among Slovenian Women After the Introduction of HPV Vaccination

Run by University Medical Centre Ljubljana · NCT06995157 · Data updated 2026-11-12

This study is trying to see if offering the HPV vaccine along with screenings can help improve vaccination rates and reduce HPV infections among women in Slovenia.

More Cervical Cancer Screening trials

Quick facts

Study typeInterventional
AgesAny age to 35 Years
SexWomen only
Enrollment500 (estimated)
SponsorUniversity Medical Centre Ljubljana
Academic / other
Locations1 site (Ljubljana, Municipality of Domžale)
StatusRecruiting
StartedSeptember 1, 2023
Main results expectedSeptember 1, 2025
Study endsApril 1, 2026
Registry record updatedMay 29, 2025
Trial IDNCT06995157 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are Slovenian women who are eligible for cervical cancer screening and have not been vaccinated against HPV.

Probably not a fit

Patients who are currently pregnant, experiencing menstrual bleeding, or have undergone a hysterectomy may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the characteristics of HPV infections and the attitudes towards HPV vaccination among women in Slovenia following the introduction of the HPV vaccine. It aims to address the low vaccination uptake and improve cervical cancer screening rates by targeting women who are in between vaccinated and unvaccinated cohorts. The study will offer the HPV vaccine to eligible participants while simultaneously conducting HPV screenings to assess the effectiveness of this combined approach. The findings could inform public health strategies to enhance vaccination coverage and reduce HPV transmission.

Why it matters

Potential benefit: If successful, this study could lead to increased HPV vaccination rates and improved cervical cancer screening, ultimately reducing the incidence of cervical cancer.

How similar studies have gone: Previous studies in Sweden have shown success with similar combined interventions, indicating a potential for effective outcomes in this study.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* regular cervical smear (CS) every 3 years after a previously normal CS result, first CS at entry into the ZORA screening program, second CS one year after entering the ZORA screening program following a previously normal first CS, control CS after a pathological cytological result or after a non-neoplastic cytological result or after conization or laser vaporization of the cervix, and curative CS due to signs or pathological clinical findings

Exclusion Criteria:

* pregnancy at the time of the gynecological examination, menstrual bleeding at the time of the gynecological examination, inflammation of the vagina and/or cervix at the time of the gynecological examination, other medical and clinical conditions that prevent the taking of a CS, condition after hysterectomy, already taken CS for the purpose of the present study, and hypersensitivity to the active substances or any excipient of the HPV vaccine

Where it's running

  • UMC Ljubljana
    Ljubljana, Municipality of Domžale, Slovenia
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.