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About
To observe the outcomes of nsPFA therapy to treat benign thyroid nodules.
Full description
Primary Objectives
• To evaluate the thyroid nodule volume changes over time in participants undergoing nsPFA as part of routine clinical care
Secondary Objectives
Enrollment
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Volunteers
Inclusion and exclusion criteria
Eligibility Criteria
Scheduled to undergo ultrasound guided nsPFA as standard of care
Age 18 to 80 years.
Capable of providing independent consent.
Presence of biopsy-confirmed benign thyroid nodule , defined as one of the following:
Nodule measuring >2cm in greatest dimension
Presence of compressive symptoms reasonably attributable to thyroid nodule (i.e. pressure sensation, dysphagia, dysphonia, respiratory distress)
No abnormal cervical lymph nodes during screening visit .
Exclusion Criteria
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Central trial contact
Victoria E Banuchi, MD
Data sourced from clinicaltrials.gov
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