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A Study of Contrast-Enhanced Mammography (CEM) Scans in People With Breast Cancer

Recruiting
18 years of age
Female
Phase N/A

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Overview

The purpose of this study is to find out whether Contrast-Enhanced Mammography/CEM scans performed 2 minutes and 6 minutes after receiving Iohexol contrast dye can be used to identify the amount of residual disease in the breast following neoadjuvant treatment.

Eligibility

Inclusion Criteria:

  • Any women >18 years of age at time of informed consent
  • Diagnosed with breast cancer and schedule for NAT

Exclusion Criteria:

  • History of kidney disease, creatinine level >1.3 or eGFR <45.
  • Known allergic reaction to gadolinium or iodinated contrast media.
  • Contraindication to contrast-enhanced breast MRI.
  • Lesion not included in the field of view of either pre- or post-NAT MRI or CEM
  • Presence of pacemakers or automated implantable cardioverter defibrilator
  • Pregnant women

Study details

Breast Cancer

NCT05990478

Memorial Sloan Kettering Cancer Center

26 January 2024

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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