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DWIBS-MRI: An Adjunct to the Traditional Diagnostic Breast Imaging Evaluation

Baylor Scott and White Health (BSWH) logo

Baylor Scott and White Health (BSWH)

Status

Unknown

Conditions

Breast Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT04491864
018-781

Details and patient eligibility

About

1.1. Primary Objectives

  • To determine if MRI DWIBS can accurately identify suspicious lesions previously categorized on mammography and sonography as potentially malignant.
  • We will also validate whether DWIBS-MRI ADC values can be used to accurately differentiate benign from malignant lesions. Additionally, because it is not known whether tumor type or growth rate (Ki67 values) will affect our results, we will include these parameters in our analysis.
  • Once we validate the use of DWIBS-MRI ADC values to determine malignancy, can we establish an ADC threshold value to decrease the number of false positive biopsies that are performed while still maintaining a zero false negative rate?
  • This study will also assess the correlation between ADC values and the Ki-67 proliferative index of malignant lesions.

Enrollment

200 estimated patients

Sex

Female

Ages

30+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • A patient will be eligible for inclusion in this study if she meets all of the following criteria:

    1. >30 years of age
    2. Genetic Female
    3. Suspected diagnosis of BIRADS 4 or BIRADS 5 masses and/or asymmetries greater than 1 centimeter based on standard 2D/3D mammogram and ultrasound imaging.

Exclusion criteria

  • A patient is ineligible for inclusion in this study if she meets any of the following criteria:

    1. Prior biopsy of suspicious lesion
    2. Breast implants
    3. Prior history of breast cancer
    4. Patient has a pacemaker
    5. Contraindications to use of MRI imaging (metal implants, etc.)
    6. Woman pregnant or lactating
    7. Calcifications as only findings present for a suspicious lesion

Trial contacts and locations

1

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Central trial contact

Mariana Hurutado, RN

Data sourced from clinicaltrials.gov

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