Actively Recruiting

All Genders
NCT04050423

Investigation of Ultrasound Imaging and Spectroscopy for Characterizing Breast Masses

Led by Sunnybrook Health Sciences Centre · Updated on 2023-12-14

1200

Participants Needed

1

Research Sites

779 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Our objective in this study is to identify an optimal set of quantitative ultrasound parameters that can be used, non-invasively, to characterize breast masses with high accuracy, as determined histopathologically. Breast cancer is the most frequent form of non-epithelial cancer diagnosed in women, with approximately 1.5 million new cases diagnosed annually worldwide. Accurate diagnosis and characterization of disease play an important role in therapy planning for breast cancer treatment. Currently, the gold standard method of tumour diagnosis is pathological examination of core biopsy specimens. However, the invasive core biopsies can cause post-surgical complications. Besides, some lesions require repeat biopsy due to sampling errors during the initial biopsy. Also X-ray mammography and ultrasound B-mode images, which are used by radiologists for breast examination, lack reliable information about micro-structural properties of tissues. There is an urgent need of a non-invasive imaging modality that can provide rapid and quantitative information for breast tumour characterization, in real time and at the patient bed. The main goal, as described above, is to select the best quantitative ultrasound parameters that can facilitate breast cancer characterization, non-invasively.

CONDITIONS

Official Title

Investigation of Ultrasound Imaging and Spectroscopy for Characterizing Breast Masses

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Women or men with suspected breast cancer
  • Ability to understand and willingness to sign a written informed consent document
Not Eligible

You will not qualify if you...

  • Chemotherapy, radiotherapy, or major surgery within 4 weeks before study registration or ongoing adverse events from such treatments
  • Receiving any other investigational agents
  • Any unstable condition that could risk patient safety or study compliance

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Trial Site Locations

Total: 1 location

1

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada, M4N 3M5

Actively Recruiting

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Research Team

G

Gregory J Czarnota, PhD, MD

CONTACT

S

Schontal Halstead

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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