search
Back to results

Ultrasound and Cytological Evaluation 3 Years After Radiofrequency Thermal Ablation of Benign Thyroid Nodules : a Prospective Exploratory Cohort of 180 Nodules (CYTOTHYRAF)

Primary Purpose

Thermal Ablation, Fine Needle Aspiration Biopsy, Thyroid Nodules

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Fine needle aspiration biopsy (FNAB)
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Thermal Ablation

Eligibility Criteria

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

Inclusion Criteria: Patients > 18 years old Carrier of a benign thyroid nodule that has undergone radiofrequency thermoablation 36 months previously ± 12 months, whether the nodule is stable, progressing or decreasing in volume during the screening period and/or on the day of inclusion. Obtaining written informed consent Affiliation to a social security system (excluding AME) Exclusion Criteria: Pregnant or breastfeeding women Previous alcohol use Patients on anti-vitamin K anticoagulants Patients on direct oral anticoagulants Persons deprived of liberty by judicial or administrative decision Persons under forced psychiatric care Persons admitted to a health or social institution for purposes other than research Persons of full age who are under legal protection (guardianship or curatorship) Persons unable to express their consent Persons under a legal protection measure (there can be no derogation for this category)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Patients with nodules treated by thermal ablation

    Arm Description

    The study population is a monocentric cohort of patients who underwent thermoablation treatment for benign thyroid nodules 3 years ago. These patients aged >18 years-old were carriers of a benign but troublesome thyroid nodule before thermal ablation, either unique or "dominant", i.e. associated with one or more other non-significant nodules (<20 mm) that were subjected to simple ultrasound surveillance. Patients refused, after clear and fair information, surgical management of their nodule. On average, 2 patients have been treated for TA per week in the Thyroid Disease and Endocrine Tumor Department since 2016. Patients systematically benefit from annual clinical and ultrasound monitoring as part of their follow-up in our Department.

    Outcomes

    Primary Outcome Measures

    Cytological change after thermoablation, as described by the 2017 Bethesda classification in six classes, scale ranging from I to VI.
    Cytological result of the nodule 3 years after thermoablation, the result of which is given according to the 2017 Bethesda classification in six classes ranging from I to VI.

    Secondary Outcome Measures

    Ultrasound description of the nodule: size (length x width x thickness)
    Ultrasound description of the nodule: volume (length x width x thickness)
    Ultrasound description of the nodule: echogenicity, as compared with the adjacent thyroid and muscular tissues
    Ultrasound description of the nodule: echostructure, measured as the percentage of liquid volume compared to nodule's total volume

    Full Information

    First Posted
    January 12, 2023
    Last Updated
    February 3, 2023
    Sponsor
    Assistance Publique - Hôpitaux de Paris
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05726981
    Brief Title
    Ultrasound and Cytological Evaluation 3 Years After Radiofrequency Thermal Ablation of Benign Thyroid Nodules : a Prospective Exploratory Cohort of 180 Nodules
    Acronym
    CYTOTHYRAF
    Official Title
    Ultrasound and Cytological Evaluation 3 Years After Radiofrequency Thermal Ablation of Benign Thyroid Nodules : a Prospective Exploratory Cohort of 180 Nodules
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 2023 (Anticipated)
    Primary Completion Date
    January 2025 (Anticipated)
    Study Completion Date
    January 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Assistance Publique - Hôpitaux de Paris

    4. Oversight

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

    5. Study Description

    Brief Summary
    There is no scientific data on post-thermal ablation cytological aspects, but treated nodules that grow back significantly after a procedure justify a new cytology in order not to ignore a neoplastic process. The EU-TIRADS classification usually used to stratify the risk of cancer (and to justify a fine needle aspiration biopsy) of thyroid nodules is not validated for nodules treated by thermal ablation (TA) (post-RF nodules). However, these nodules often acquire ultrasound criteria of suspicion making it necessary to develop an ultrasound stratification of the risk of malignancy specific to nodules treated by TA. The objective of this work is to describe the ultrasound and cytological aspects of these treated nodules by performing a systematic assessment at 3 years after thermal ablation including systematic neck ultrasound and fine needle aspiration biopsy. Thus, an ultrasound and cytological atlas (Bethesda classification 2017) of nodules treated by thermal ablation will be constituted.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Thermal Ablation, Fine Needle Aspiration Biopsy, Thyroid Nodules

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Patients with nodules treated by thermal ablation
    Arm Type
    Experimental
    Arm Description
    The study population is a monocentric cohort of patients who underwent thermoablation treatment for benign thyroid nodules 3 years ago. These patients aged >18 years-old were carriers of a benign but troublesome thyroid nodule before thermal ablation, either unique or "dominant", i.e. associated with one or more other non-significant nodules (<20 mm) that were subjected to simple ultrasound surveillance. Patients refused, after clear and fair information, surgical management of their nodule. On average, 2 patients have been treated for TA per week in the Thyroid Disease and Endocrine Tumor Department since 2016. Patients systematically benefit from annual clinical and ultrasound monitoring as part of their follow-up in our Department.
    Intervention Type
    Procedure
    Intervention Name(s)
    Fine needle aspiration biopsy (FNAB)
    Intervention Description
    Thyroid FNAB is a minimally invasive procedure performed routinely by an experienced sonographer. It is a safe and brief procedure, performed with a 27G or 25G (very fine) needle (3 needles, i.e. 1 needle per pass)
    Primary Outcome Measure Information:
    Title
    Cytological change after thermoablation, as described by the 2017 Bethesda classification in six classes, scale ranging from I to VI.
    Description
    Cytological result of the nodule 3 years after thermoablation, the result of which is given according to the 2017 Bethesda classification in six classes ranging from I to VI.
    Time Frame
    Day of the Fine Needle Aspiration Biopsy
    Secondary Outcome Measure Information:
    Title
    Ultrasound description of the nodule: size (length x width x thickness)
    Time Frame
    Day of the Fine Needle Aspiration Biopsy
    Title
    Ultrasound description of the nodule: volume (length x width x thickness)
    Time Frame
    Day of the Fine Needle Aspiration Biopsy
    Title
    Ultrasound description of the nodule: echogenicity, as compared with the adjacent thyroid and muscular tissues
    Time Frame
    Day of the Fine Needle Aspiration Biopsy
    Title
    Ultrasound description of the nodule: echostructure, measured as the percentage of liquid volume compared to nodule's total volume
    Time Frame
    Day of the Fine Needle Aspiration Biopsy

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients > 18 years old Carrier of a benign thyroid nodule that has undergone radiofrequency thermoablation 36 months previously ± 12 months, whether the nodule is stable, progressing or decreasing in volume during the screening period and/or on the day of inclusion. Obtaining written informed consent Affiliation to a social security system (excluding AME) Exclusion Criteria: Pregnant or breastfeeding women Previous alcohol use Patients on anti-vitamin K anticoagulants Patients on direct oral anticoagulants Persons deprived of liberty by judicial or administrative decision Persons under forced psychiatric care Persons admitted to a health or social institution for purposes other than research Persons of full age who are under legal protection (guardianship or curatorship) Persons unable to express their consent Persons under a legal protection measure (there can be no derogation for this category)
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Adrien BEN HAMOU, MD-PhD
    Phone
    01 84 82 77 59
    Ext
    +33
    Email
    adrien.benhamou@hotmail.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Camille BUFFET, MD-PhD
    Phone
    01 84 82 77 59
    Ext
    +33
    Email
    camille.buffet@aphp.fr

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Ultrasound and Cytological Evaluation 3 Years After Radiofrequency Thermal Ablation of Benign Thyroid Nodules : a Prospective Exploratory Cohort of 180 Nodules

    We'll reach out to this number within 24 hrs