Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
44 participants
INTERVENTIONAL
2024-03-12
2025-12-30
Brief Summary
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Detailed Description
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Most evidence supporting RFA of thyroid nodules comes from international cohorts. In a recent meta-analysis, RFA accomplished volume reduction ranging from 68 to 87% in over 1100 treated nodules. This reduction was sustained for up to 5 years. In terms of its safety, a recent systematic review of 2700 nodules showed only 41 major complications and 48 minor complications from RFA. Of note, most complications were transient, only 4 patients developed permanent voice changes, while 1 required rescue lobectomy after a nodule ruptured. Published data in the United States also showed RFA to be an effective and safe strategy. However, of the 47 studied patients, none were LatinX. Furthermore, lack of coverage by insurance companies means this procedure is typically only available as an out-of-pocket expense and is therefore out of reach for underserved patients. Data to establish the safety/feasibility of this novel intervention is needed for the LatinX population.
Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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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
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
Interventions
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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
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
90 Years
ALL
No
Sponsors
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Northwell Health
OTHER
Responsible Party
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Daniel Kuriloff
Director, Center for Thyroid & Parathyroid Surgery
Principal Investigators
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Daniel Kuriloff, MD
Role: PRINCIPAL_INVESTIGATOR
Northwell Health
Locations
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Northwell Health Physician Partners
New York, New York, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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22-0711
Identifier Type: -
Identifier Source: org_study_id
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