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

  • STATUS
    Recruiting
  • participants needed
    150
  • sponsor
    Guardant Health, Inc.
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Updated on 19 February 2024
See if I qualify
cancer
breast cancer

Summary

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.

Details
Condition Advanced Breast Cancer
Age 18years - 100years
Treatment Guardant360 test
Clinical Study IdentifierNCT04436393
SponsorGuardant Health, Inc.
Last Modified on19 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

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

Exclusion Criteria

Unable to understand English
Clear my responses
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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