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Clinical Trials in Sweden / NCT05229679
Recruiting Not applicable

HPV-based Screening Among Women 23-29 Years of Age

NCT05229679 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2020-11-16
Last updated
2025-03-19

Condition(s) studied

Human Papilloma VirusCervical Intraepithelial NeoplasiaCervical Cancer

Investigational drug(s) / intervention(s)

HPV testing

HPV testing: All women age 23-29 resident in the pilot counties will be invited to HPV screening as of the study start date. The same invitation as currently used for women aged 30 and upwards will be used. This information clearly states that it is possible to opt out of the program and that data from the screening program will be collected to regional and national quality registers who will systematically evaluate the quality of the care. At the screening station, the samples are collected identically regardless of primary screening test used - there is no change in the procedures used neither for the woman or for the midwives taking the sample. HPV testing will be performed using the same purchased, CE-marked and accredited HPV screening platforms as currently used for women aged 30 and upwards. The cytology is according to the liquid-based cytology method.

Study summary

The aim of the trial is to determine whether organized screening with primary HPV analysis provide higher cancer protection in the age group 23-29 years compared to primary cytology.

Eligibility

Sex
FEMALE
Min age
23 Years
Max age
29 Years
Healthy volunteers
No
Inclusion Criteria: * Women ages 23-29 invited to screening. Exclusion Criteria: * Women who do not show up for screening or do not consent.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Region of Skåne Lund Skåne County Active Not Recruiting
Region Stockholm Stockholm Sweden Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05229679 on ClinicalTrials.gov ↗ ← All trials in Sweden