CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 250 enrolled
Drug / intervention
FFDM +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02306265
NCT02306265N/ACompleted

Assessment of Diagnostic Accuracy and Performance of Digital Breast Tomosynthesis Compared to Mammography (ADAPT Trial) ADAPT-SCR: Recruitment Plan for Asymptomatic Women Undergoing Screening Mammography

GE Healthcare·interventional·Posted Dec 3, 2014·Updated Jan 29, 2019

In Brief

A clinical study evaluating FFDM and DBT for Breast Cancer and 2 related conditions. Completed, enrolled 250 participants across 2 sites.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedDec 3, 2014
Enrollment StartMay 1, 2015
Primary CompletionJul 7, 2017
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 11.6 years ago

Interventions

FFDMdevice

2D imaging of the breast using Full-Field Digital Mammography (FFDM) device

DBTdevice

3D imaging of the breast using Digital Breast Tomosynthesis (DBT) device