Clinical Trial

PERsonalized Mammographic Screening in Norway

Study acronym: PERMS
Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
The aim of this study is to assess attendance among women invited to additional breast imaging because they were identified as having an increased risk of breast cancer at screening. High-risk women were defined in two studies: Study A; women with high mammographic density, representing approximately 3-5% of screened women, and Study B; women with a false-positive screening result. Women in Study A will be offered an additional screening examination with digital breast tomosynthesis immediately within 6 months after the screening examination. Women in Study B will be offered an additional standard digital mammography examination one year after their initial screening.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-23.
Trial Details
NCT Number NCT07371702
Lead Sponsor Norwegian Institute of Public Health
Collaborators: Norwegian Cancer Society, University Hospital, Akershus, Oslo University Hospital, Vestre Viken Hospital Trust
Conditions Breast Cancer, Mammographic Breast Density, Risk Stratification
Enrollment 3,000 participants
Start Date 2026-01
Primary Completion 2028-01 (estimated)
Study Completion 2033-12 (estimated)
Updated on ClinicalTrials.gov 2026-01-29