Skip to main content
OpenTrials
Completed

NCT Number: NCT02698202

Screening for Breast Cancer With Digital Breast Tomosynthesis

Randomized trial comparing the performance of tomosynthesis and 2D Digital Mammography vs 2D Digital Mammography only in respect to incidence of advanced cancers (interval and following round) and interval cancers.

Completed

Looking for future studies?

Notify Me

Key information

Age range

45 year–70 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Azienda Sanitaria Locale Reggio Emilia

Reggio Emilia, Italy

About this study

The investigators conduct a randomized trial (about 20000 tests in the intervention arm) comparing the performance of tomosynthesis plus 2D Digital Mammography vs usual care (2D digital mammography) in respect to incidence of advanced cancers (interval and following round) and interval cancers. The investigators also will measure detection rates, specificity, interval cancers, advanced cancers occurring as interval cancers or at subsequent screens and allowing to estimate overdiagnosis. In Reggio Emilia a population-based screening program is active. It invites all women from 45 to 74 years old for a 2D digital mammography (2 projections, double reading) every 2 years (annually from 45 to 49).

Women will be asked for informed consent when they attend the mammography. I they accept they will be randomised to one of the two arms.

All examinations will be read by two independent radiologists, in case of discordance a third reading is asked.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

45-70 years old women invited to breast cancer screening program who accepted to participate

Exclusion criteria

  • previous breast cancer diagnosis
  • pregnancy or suspicion of pregnancy
  • presence of BRCA1/2 gene mutation
  • Previous Digital Breast Tomosynthesis performed
  • unable to understand informed consent
  • chemotherapy in progress
  • presence of breast implant

Treatment and study plan

Digital Breast Tomosynthesis

Device

twice screening examination: standard 2D mammography + Digital Breast Tomosynthesis

Primary outcomes

  1. cumulative incidence of T2+ cancers after screening

    Time frame: 2 years

  2. incidence of interval cancers

    Time frame: 2 years

Secondary outcomes

  1. Detection rate

    Time frame: 2 years

  2. recall rate

    Time frame: baseline

  3. Positive Predictive value

    Time frame: baseline

  4. diagnostic agreement between tomosynthesis and 2d mammography

    Time frame: baseline

  5. Detection rate of in situ ductal carcinoma

    Time frame: 2 years

  6. biopsy rate

    Time frame: baseline

  7. self-reported pain and discomfort during mammography

    Time frame: baseline

  8. x-ray dose

    Time frame: baseline

Sponsors and collaborators

Lead sponsor

Azienda USL Reggio Emilia - IRCCS

Other Gov

Collaborators

  • Regione Emilia-Romagna

Registry information

Official study title

Randomized Controlled Trial to Evaluate the Efficacy of Digital Breast Tomosynthesis in Reggio Emilia Breast Cancer Screening Program in the 45-74 Age Group

Important dates

Study start
2014
Primary completion
2017
Study completion
2019
First posted
Mar 3, 2016
Registry last updated
Dec 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.