Clinical Trial: CellFX ® Percutaneous Electrode (PE) Treatment of Symptomatic Benign Thyroid Nodules
Study Status: COMPLETED
Recruit Status: COMPLETED
Condition: Thyroid Nodule (Benign)
Study Type: INTERVENTIONAL
Official Title: First Clinical Feasibility Study Using the CellFX® Percutaneous Electrode (PE) System for the Treatment of Symptomatic Benign Thyroid Nodules
Brief Summary:
The objective of this clinical feasibility study is to evaluate initial clinical safety and device performance of the CellFX Percutaneous Electrode (PE) System for the treatment of symptomatic benign thyroid nodules.
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