Which thyroid test spares more patients from unneeded surgery?
NCT ID NCT02681328
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study compares two genetic tests, Afirma GSC and ThyroSeq v.3, on tissue from thyroid nodules that have unclear biopsy results. The goal is to see which test better identifies benign nodules, so patients can avoid unnecessary surgery. About 328 participants with indeterminate thyroid nodules are enrolled. The results could help doctors choose the best test to preserve quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Molecular diagnostic tests (Afirma GSC and ThyroSeq v.3) on thyroid tissue
- What this could lead to
- If successful, this could help doctors more accurately identify which thyroid nodules are benign, allowing many patients to safely avoid surgery and preserve their quality of life.
- What could go wrong
- This is a diagnostic comparison study, not a treatment trial. The tests may not perform as hoped, and results may not apply to all patients or settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
328 people
The number who actually took part.
- Started
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May 2016
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients undergoing thyroid fine needle aspiration (FNA) within the University of California, Los Angeles (UCLA) Health System
- Ages
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18 to 100 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with a thyroid nodule who have a thyroid biopsy performed at UCLA health will be eligible for the study and consented if they agree to participate. * Patients who have an indeterminate FNA biopsy result (Bethesda category 3 or 4) will be enrolled in the study if they agree to participate. Exclusion Criteria: * Patients who do not have an indeterminate biopsy result (either patients who have a benign, insufficient, or malignant result).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Jonsson Comprehensive Cancer Center at UCLA
Los Angeles, California, 90095-1781, United States
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