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NCT02306265 · ClinicalTrials.gov registry record · NA

Assessment of Diagnostic Accuracy and Performance of Digital Breast Tomosynthesis Compared to Mammography

A NA study, sponsored by GE Healthcare.

Completed
Registry status
NA
Development phase
250
Enrollment target

NCT02306265: Completed NA study, sponsored by GE Healthcare.

NCT02306265 is a NA study that has completed, run by GE Healthcare. The registered enrollment target is 250 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02306265, a NA study, has completed, sponsored by GE Healthcare.

COMPLETED
Registry status
NA
Development phase
250 participants
Enrollment target

Study Summary

The aim of this recruitment plan (ADAPT-SCR) is to collect image and other data on both digital breast tomosynthesis (DBT) and full-field digital mammography (FFDM) from asymptomatic women undergoing screening mammography.

Primary Outcome

Collect breast image data using two (2) methods: Digital Breast Tomosynthesis (DBT) and Full Field Digital Mammography (FFDM) from asymptomatic women undergoing screening mammography.

Interventions

  • DEVICE FFDM
  • DEVICE DBT

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2015-05
Est. Completion 2017-07-07
Phase NA
GE Healthcare

99 total trials

What the finished NCT02306265 record still lists

NCT02306265 is an interventional study that assigns participants to a tested intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 2 interventions - of which FFDM is the first listed.

NCT02306265 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02306265 about?

NCT02306265 is a clinical study titled "Assessment of Diagnostic Accuracy and Performance of Digital Breast Tomosynthesis Compared to Mammography". The aim of this recruitment plan (ADAPT-SCR) is to collect image and other data on both digital breast tomosynthesis (DBT) and full-field digital mammography (FFDM) from asymptomatic women undergoing screening mammography.

What is the current status of trial NCT02306265?

This trial is currently completed. It is a NA study. The enrollment target is 250 participants. The study started on 2015-05. Estimated completion is 2017-07-07.

What interventions are being tested in trial NCT02306265?

The interventions under investigation include: FFDM (DEVICE), DBT (DEVICE).

Who is sponsoring clinical trial NCT02306265?

This trial is sponsored by GE Healthcare, which has 99 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02306265's enrollment target sits among peer trials

250 410th of 2000 higher than 1,567 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02306265, the US trial registry maintained by the National Library of Medicine. NCT02306265 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.