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

  • STATUS
    Recruiting
  • participants needed
    150
  • sponsor
    Guardant Health, Inc.
Send
Updated on 5 August 2020
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 on5 August 2020

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
Read more

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

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.

Learn more

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

Learn more

Similar trials to consider

Browse trials for

cancer
breast cancer

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.