Patient-Assisted Compression in 3D - Impact on Image Quality and Workflow
Completed · Not applicable
Conditions studied: Breast Cancer
In brief
Patient-assisted compression (PAC) allows the patient to participate in controlling the amount of compression force during mammography and is a personalized approach that has demonstrated successful reduction in discomfort experienced during mammography. General Electric Healthcare's Senographe Pristina, an innovative mammography platform that provides both two-dimensional (2D) and three-dimensional (3D) imaging capabilities, offers both standard and patient-assisted compression modes. This study will evaluate image quality and clinical workflow as it relates to use of PAC with the Senographe Pristina 3D.
Key facts
- Study ID
- NCT03456427
- Run by
- GE Healthcare
- People needed
- 36
- Starts
- 2018-01-04
- Expected to finish
- 2018-01-09
- Last updated by the study team
- 2019-04-05
Who can join
Age: 40 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Are women aged 40 years or older;
- Are asymptomatic and scheduled for screening mammography;
- Have left and right breasts;
- Have breast sizes compatible with the dimensions of a 24 x 31 cm image detector, without anatomical cut-off;
- Are documented as non-pregnant based on the investigator's medical judgment and in consideration of local clinical practice standards for evidence of non-pregnancy;
- Are able and willing to comply with study procedures; and
- Are able and willing to provide written informed consent to participate.
You may not qualify if…
- Are women aged 40 years or older;
- Are asymptomatic and scheduled for screening mammography;
- Have left and right breasts;
- Have breast sizes compatible with the dimensions of a 24 x 31 cm image detector, without anatomical cut-off;
- Are documented as non-pregnant based on the investigator's medical judgment and in consideration of local clinical practice standards for evidence of non-pregnancy;
- Are able and willing to comply with study procedures; and
- Are able and willing to provide written informed consent to participate.
Where it is running
- Boca Raton Regional Hospital — Boca Raton, Florida, United States
Full record on ClinicalTrials.gov
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