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Guardant360 Related Clinical Outcomes in Patients Who Share Medical Records-Breast Cancer

Guardant360 Related Clinical Outcomes in Patients Who Share Medical Records-Breast Cancer

Recruiting
18 years and older
All
Phase N/A

Overview

The purpose of this study is to observe the routine clinical care of patients who have been diagnosed with breast cancer and have undergone Guardant360 testing.

Description

Patients who have been diagnosed with breast cancer and have undergone Guardant360 testing will be approached regarding participation in the study. After being informed about the study and potential risks, all patients providing informed consent and access to their medical records, will provide a list of their health care providers related to their cancer treatment. Data related to their routine clinical care will be abstracted from medical records.

Eligibility

Inclusion Criteria:

  1. Adults (18 years of age and older) with a diagnosis of breast cancer
  2. Guardant360 test results released to the patient's physician no less than 14 days prior to initial patient contact
  3. Patient has previously provided contact information (either email or phone) to Guardant Health
  4. Able and willing to complete the electronic informed consent process
  5. Must have access to a computer terminal or personal computing device
  6. Willingness to consent to the release of medical records

Exclusion Criteria:

  1. Unable to understand English

Study details
    Advanced Breast Cancer

NCT04436393

Guardant Health, Inc.

5 August 2020

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FAQs

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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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