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About
To track the outcomes of patients who have been treated with RFA and its long-term effectiveness, and to learn more about the quality of life of patients who have received RFA in this study.
Full description
Primary Objectives
• To evaluate thyroid nodule volume changes over time in participants undergoing RFA as part of clinical care
Secondary Objectives
Enrollment
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Inclusion and exclusion criteria
Eligibility Criteria
Participants scheduled to undergo ultrasound-guided RFA for the following conditions: benign thyroid nodules, indeterminate thyroid nodules, low-risk DTC, and recurrent PTC
Participant is over 18 years and is either not a surgical candidate or has declined surgery.
Capable and willing to provide written informed consent
Participant has one of the following diagnoses:
Exclusion Criteria
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Central trial contact
Victoria E Banuchi, MD
Data sourced from clinicaltrials.gov
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