Lung Cancer Clinical Trial
Official title:
A Pilot Study to Isolate and Test Circulating Tumor Cells Using the ClearCell® FX EP+ System
Verified date | March 2018 |
Source | Mayo Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to isolate and measure circulating tumor cells in the blood stream to advance detection of cancer and treatment monitoring. In this study, the investigators will utilize the novel technology for circulating tumor cell detection in order to evaluate their presence in patients with lung cancer.
Status | Completed |
Enrollment | 23 |
Est. completion date | July 9, 2016 |
Est. primary completion date | July 9, 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Stage IB and above non-small cell lung cancer or metastatic lung cancer - Age >18 years old - Willing and able to consent to study - No prior history of neoadjuvant therapy. Exclusion Criteria: - Age <18 years old - Unable to provide consent |
Country | Name | City | State |
---|---|---|---|
United States | Mayo Clinic in Rochester | Rochester | Minnesota |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic | Clearbridge Biomedics |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number and types of mutations in the primary tumor. | Within 1 year | ||
Primary | Number and type of mutations detectable in the matched circulating tumor cell samples. | Within 1 year | ||
Secondary | Concordance of mutations detected by either method. | Within 1 year |
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