Actively Recruiting

Phase Not Applicable
Age: 50Years - 69Years
FEMALE
Healthy Volunteers
NCT06032390

Artificial Intelligence in Mammography Screening in Norway

Led by Norwegian Institute of Public Health · Updated on 2026-01-14

150000

Participants Needed

1

Research Sites

444 weeks

Total Duration

On this page

Sponsors

N

Norwegian Institute of Public Health

Lead Sponsor

H

Helse Vest

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this randomized controlled trial is to compare the number of breast cancers detected among women who had their screening mammograms interpreted by artificial intelligence (AI) in combination with one or two breast radiologists to the number of breast cancers detected after standard independent double reading in BreastScreen Norway. The aims of the study is to prove that screening interpretation with AI in combination with one or two radiologists (the intervention) is non-inferior to standard interpretation procedure.

CONDITIONS

Official Title

Artificial Intelligence in Mammography Screening in Norway

Who Can Participate

Age: 50Years - 69Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Women attending the population-based mammography screening program BreastScreen Norway providing a signed, informed consent
Not Eligible

You will not qualify if you...

  • Women attending the population-based mammography screening program BreastScreen Norway not providing a signed, informed consent

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Trial Site Locations

Total: 1 location

1

Cancer Registry of Norway, Norwegian Institute of Public Health

Oslo, Norway

Actively Recruiting

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Research Team

S

Solveig Hofvind, PhD

CONTACT

Å

Åsne S Holen, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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