Radiofrequency Ablation Study in LatinX Patients
Thyroid Nodule
About this trial
This is an interventional diagnostic trial for Thyroid Nodule
Eligibility Criteria
Inclusion Criteria: Subject capable of giving informed consent Stated willingness to comply with all study procedures and availability for the duration of the study Subjects over 18 years of age Subject who self-identifies as LatinX Subjects who have a benign, symptomatic thyroid nodule Subjects whose nodule has well-defined margin on ultrasound and is surrounded by at least 2mm of normal thyroid parenchyma in all directions Exclusion Criteria: Patients who are pregnant, trying to become pregnant, or breastfeeding Patient who have a cardiac pacemaker,defibrillator , or other electromedical equipment Patients who have a nodule that is malignant or not predominantly solid (must be >50% solid by ultrasound) Patients who cannot give consent Patients on anticoagulation or dual antiplatelet therapy Patients with acute illness People with BP > 140/90 prior to the scheduled procedure
Sites / Locations
- Northwell Health Physician PartnersRecruiting
Arms of the Study
Arm 1
Experimental
Mygen V-1000 RF system
The Mygen V-1000, a microprocessor-based generator of RF Medical Co., Ltd., provides up to 140 watts of radio-frequency (RF) energy to be used for coagulation & ablation of vessel, tissue & bone