Guardant360 Related Clinical Outcomes in Patients Who Share Medical Records-Breast Cancer
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- STATUS
- Recruiting
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- participants needed
- 150
-
- sponsor
- Guardant Health, Inc.
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 | 18-100 years |
| Treatment | Guardant360 test |
| Clinical Study Identifier | NCT04436393 |
| Sponsor | Guardant Health, Inc. |
| Last Modified on | 19 February 2024 |
How to participate?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf 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 moreComplete 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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