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Radiofrequency Ablation Study in LatinX Patients

Primary Purpose

Thyroid Nodule

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mygen V-1000 RF system
Sponsored by
Northwell Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Thyroid Nodule

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Arm Label

Mygen V-1000 RF system

Arm Description

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

Outcomes

Primary Outcome Measures

Number of participants with treatment-related changes in thyroid nodule volumes
To study the change in nodule volume

Secondary Outcome Measures

Full Information

First Posted
May 19, 2023
Last Updated
October 10, 2023
Sponsor
Northwell Health
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1. Study Identification

Unique Protocol Identification Number
NCT05903196
Brief Title
Radiofrequency Ablation Study in LatinX Patients
Official Title
Study of the Use of Radiofrequency Ablation in LatinX Patients With Symptomatic Benign Thyroid Nodules
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 31, 2023 (Anticipated)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
September 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwell Health

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Benign thyroid nodules can still create cosmetic, compressive, or hormonal issues for patients. In the past, surgery was typically used to treat thyroid nodules causing the above issues through partial or complete thyroidectomy. More recently, minimally-invasive techniques have been developed to treat these issues. This study is investigating the use of one of these techniques, radiofrequency ablation, in Latinx patients with benign symptomatic thyroid nodules. This procedure is of interest because it avoids the risks of surgery and can be done outside an operating room. The study hypothesis is that the use of RFA is an effective and safe therapeutic option for LatinX patients with a symptomatic benign nodule wishing to avoid surgery.
Detailed Description
Thyroid nodules can create issues for individuals such as affecting the level of their thyroid hormones, causing an unwanted physical appearance, or pressing on other important structures in the neck (for example, trachea and esophagus). In the past, surgery was typically used to treat thyroid nodules causing the above issues, either taking out some or all of the thyroid. More recently, new techniques that do not require surgery have been developed to treat these issues. This study is investigating the use of one of these newer techniques, called radiofrequency ablation in Latinx patients with non-cancerous symptomatic thyroid nodules. This procedure is of interest because it avoids the risks of surgery (like bleeding, infection, scars) and can be done in a clinic setting. The theory is that this procedure will be a safe and effective alternative to surgery for non-cancerous thyroid nodules that are causing symptoms in Latinx patients, which is a population in which this treatment has not yet been studied. Patients who decide to enroll in the study will be required to fill out questionnaires, have blood tests, have ultrasounds of the thyroid, and undergo the radiofrequency ablation minimally-invasive treatment instead of surgery. Patients will be evaluated at 1 month, 3 months, 6 months, 12 months, and 18 months after the procedure to assess for effectiveness of the procedure and any side effects. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thyroid Nodule

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
44 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mygen V-1000 RF system
Arm Type
Experimental
Arm Description
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
Intervention Type
Device
Intervention Name(s)
Mygen V-1000 RF system
Intervention Description
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
Primary Outcome Measure Information:
Title
Number of participants with treatment-related changes in thyroid nodule volumes
Description
To study the change in nodule volume
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Karina Ziskovich, BBA
Phone
212-434-3715
Email
kziskovich@northwell.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jose Sanchez, MD
Phone
212-434-4972
Email
jsanchez17@northwell.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Kuriloff, MD
Organizational Affiliation
Northwell Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwell Health Physician Partners
City
New York
State/Province
New York
ZIP/Postal Code
10022
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karina Ziskovich, BBA
Phone
212-434-3715
Email
kziskovich@northwell.edu
First Name & Middle Initial & Last Name & Degree
Jose Sanchez Escobar, MD
Phone
212-434-4972
Email
jsanchez17@northwell.edu

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Radiofrequency Ablation Study in LatinX Patients

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