No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
29 – 85
Sex
Any
Study type
Observational
Participants needed
2,400 (estimated)
Sponsor
Veracyte, Inc. · Industry
Who this trial is looking for
This trial is looking for adults aged 29 to 85 with a recently found lung nodule. Participants will provide a nasal swab to help doctors decide on the best treatment options based on test results.
Are You a Good Fit for This Trial?
You may be able to join if
I can tolerate a nasal swab
I have signed the consent form
I have a new lung nodule found in the last 90 days
I have a CT report for my nodule
I am 29 to 85 years old
I am a current or former smoker
My lung nodule is 30 mm or smaller
You may not be able to join if
I have active cancer (except non-melanoma skin cancer)
I have had primary lung cancer before
I have participated in this study before
I am currently on treatment with an investigational device or drug
I am enrolled in another clinical trial that might affect my treatment
I am using any tools or tests for lung nodule risk assessment that are not clinically validated
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The goal of this observational study is to learn how a physician uses the results of the Percepta® Nasal Swab test to manage people with a newly identified pulmonary nodule.
The main questions it aims to answer are:
* Does the use of the Percepta Nasal swab test reduce the number of invasive procedures in people with a low-risk result and whose nodule is benign?
* Does the use of the Percepta Na…
The goal of this observational study is to learn how a physician uses the results of the Percepta® Nasal Swab test to manage people with a newly identified pulmonary nodule.
The main questions it aims to answer are:
* Does the use of the Percepta Nasal swab test reduce the number of invasive procedures in people with a low-risk result and whose nodule is benign?
* Does the use of the Percepta Nasal swab test decrease the time to treatment in people with a high-risk result and whose nodule is cancer?
Participants will be randomly assigned to either a group where the test result is provided to the physician (test arm) or to a group where the test result is not provided (control arm). Researchers will compare management of participants in the two groups.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
* Able to tolerate nasal epithelial specimen collection
* Signed written Informed Consent obtained
* Subject clinical history available for review by sponsor and regulatory agencies
* New nodule identified on imaging \< 90 days prior to nasal sample collection
* CT report availa…
Inclusion Criteria:
* Able to tolerate nasal epithelial specimen collection
* Signed written Informed Consent obtained
* Subject clinical history available for review by sponsor and regulatory agencies
* New nodule identified on imaging \< 90 days prior to nasal sample collection
* CT report available for index nodule
* 29 - 85 years of age
* Current or former smoker (\>100 cigarettes in a lifetime)
* Pulmonary nodule ≤30 mm detected by CT
Exclusion Criteria:
* Active cancer (other than non-melanoma skin cancer)
* Prior primary lung cancer (prior non-lung cancer acceptable)
* Prior participation in this study (i.e., subjects may not be enrolled more than once)
* Current active treatment with an investigational device or drug
* Patient enrolled or planned to be enrolled in another clinical trial that may influence management of the patient's nodule
* Concurrent or planned use of tools or tests for assigning lung nodule risk of malignancy other than clinically validated risk calculators
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