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Efficacy and Safety of RFA vs MWA for Treatment of Large Benign Thyroid Nodules, RCT

31 augustus 2026 bijgewerkt door: Man Him Matrix Fung, The University of Hong Kong

Comparing the Efficacy and Safety of Radiofrequency Ablation Versus Microwave Ablation for the Treatment of Large Benign Thyroid Nodules, a Randomized Controlled Trial

We will conduct a multi-institutional randomized control trial of RFA and MWA for the primary treatment of large, benign nodules. Adult patients >/=18 years of age who have a solitary thyroid nodule ≥20ml in volume who presents to 1) Columbia University, NY or 2) Queen Mary Hospital, Hong Kong for consultation will be eligible for enrollment in the study. They will need either a) two benign fine needle biopsies, with the most recent biopsy performed within 1 year of enrollment in study or b) one benign fine needle biopsy and low suspicion characteristics on ultrasound. Both functional and non-functional nodules are eligible. After thorough evaluation of each individual case and if the eligibility criteria are met, participants will be offered ultrasound guided thermal ablation as a viable option for management of their nodule. If they consent to undergo thermal ablation and consent to participation in the study, patients will be randomly assigned to either treatment arm a) RFA or treatment arm b) MWA according to a pre-generated block randomization list created using www.sealedenvelope.com.

Studie Overzicht

Gedetailleerde beschrijving

There is an estimated 10% lifetime probability for developing a thyroid nodule. Although up to 15% of these nodules will prove to be malignant, most thyroid nodules that are identified are benign nodules. However, even benign nodules can continue to grow to a size that start to cause compressive symptoms for patients, including neck pressure and discomfort, dysphagia, dyspnea, and dysphonia. Some nodules will become autonomously functioning causing hyperthyroidism. Traditionally the gold standard treatment for these benign, but problematic nodules, has been thyroidectomy. Although generally a low risk operation, thyroidectomy is associated with some risk for recurrent laryngeal nerve injury, bleeding, infection, and need for thyroid hormone supplementation.

Introduced in the early 2000s, ultrasound-guided percutaneous ablation of thyroid lesions has emerged as a potential alternative to surgery in patients with benign thyroid nodules. Of the myriad ablation methods, the most commonly used technique is radiofrequency ablation (RFA). An expanding body of evidence shows that radiofrequency ablation and other percutaneous interventions are effective treatments for benign solid thyroid nodules, toxic adenomas, and thyroid cysts resulting in overall volume reduction ranges of 40-70% with durable resolution of compressive and hyperthyroid symptoms. However, RFA is not without its limitations. Radiofrequency waves can be limited by the heat sink effect and tissue char leading to longer procedure times and potentially less optimal outcomes in larger, hypervascular, and/or more cystic nodules.

Microwave ablation (MWA) is another ablative technique that uses electromagnetic energy waves to cause tissue hyperthermia and coagulative necrosis. It generally causes higher ablation temperatures than RFA and is less subject to the heat sink effect, and therefore can facilitate more efficient ablation procedures. Current evidence comparing RFA versus MWA for thyroid ablation were limited and were either retrospective or non-randomized, with focus mainly on small thyroid nodules of ≤10ml in volume. There is a lack of high quality evidence on the safety and efficacy of RFA versus MWA for the treatment of large thyroid nodules (≥20ml). Given the higher ablation temperatures, freedom from heat sink effect and no influence from impedance changes during ablation, MWA may achieve different treatment efficacy in large nodules.

The aim of this randomized controlled trial is to compare the safety and efficacy of RFA and MWA in the treatment of large, benign thyroid nodules. We hypothesize that MWA is not inferior to RFA in terms of complication rate and overall volume reduction of large, benign nodules, but will also be associated with overall decrease in procedure time and procedural discomfort. Patients with large benign thyroid nodules ≥20ml will be considered for recruitment. Suitable subjects will be randomized to receive either RFA or MWA according to a pre-generated block randomization list at a 1:1 ratio. The primary outcome of is the volume reduction rate at 6 months and one year after ablation. The secondary outcomes include safety, complication rates and quality of life after both procedures.

Studietype

Ingrijpend

Inschrijving (Geschat)

25

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

  • Naam: Man Him, Matrix Dr. Fung, MBBS
  • Telefoonnummer: +852 2255 4232
  • E-mail: mmhfung@hku.hk

Studie Locaties

      • Hong Kong, Hongkong
        • Werving
        • Queen Mary Hospital
        • Contact:
          • Man Him, Matrix Dr. Fung, MBBS
          • Telefoonnummer: +852-22554232
          • E-mail: mmhfung@hku.hk

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • who have a solitary thyroid nodule ≥20ml in volume
  • two benign fine needle biopsies, with the most recent biopsy performed within 1 year of enrollment in study or one benign fine needle biopsy and low suspicion characteristics on ultrasound
  • Both functional and non-functional nodules are eligible

Exclusion Criteria:

  • have multiple nodules and planned simultaneous ablation
  • indeterminate nodules classified benign
  • nodules with substernal extension or posterior extension that cannot be viewed sufficiently with ultrasound
  • current pregnancy or cardiac arrhythmias

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Microwave ablation
Apply microwave ablation to those large benign thyroid nodules for shrinkage purpose
Ultrasound-guided thermal ablation will be performed using ECO Medical internally cooled MWA antennas (16 or 17 gauge) powered by the ECO Medical generator in accordance with the 'moving shot' technique described by Baek et al. The MWA procedure uses image guidance to place an electrode through the skin into the target area. In MWA, high frequency electromagnetic waves are passed through an electrode, creating a small region of heat to treat the lesion.
Andere namen:
  • MWA
Experimenteel: Radiofrequency ablation
Apply radiofrequency ablation to those large benign thyroid nodules for shrinkage purpose
Ultrasound-guided thermal ablation will be performed using STARmed internally cooled RFA electrodes (18 gauge) powered by the VIVA RF generator in accordance with the 'moving shot' technique described by Baek et al. The RFA procedure uses image guidance to place an electrode through the skin into the target area. In RFA, high frequency electrical currents are passed through an electrode, creating a small region of heat to treat the lesion.
Andere namen:
  • RFA

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Volume reduction rate (VRR) of thyroid nodule at 6 months and 12 months (%)
Tijdsspanne: 6 months and 12 months
To measure the volume reduction rate (VRR) of thyroid nodule at 6-month and 12-month volume of nodule= length(cm) x width(cm) x depth(cm) x (π / 6 ) VRR = [(volume at baseline - volume at 6-month or 12-month)/volume of baseline] x 100%
6 months and 12 months
Complications from procedure including vocal cord palsy, bleeding, infection, nodule rupture, skin burn
Tijdsspanne: 12 months
To assess any complications from procedure during follow-up period after ablation
12 months

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Changes in compressive symptom scores (0-100)
Tijdsspanne: 12 months
To measure the changes in compressive symptoms scores. Compressive symptoms score is from 0 to 100. The higher score means more compressive symptom.
12 months
Changes in cosmetic symptom scores (1-4)
Tijdsspanne: 12 months

To assess the change of cosmetic symptom by experienced doctors until 12 months.

Cosmetic symptoms is from 1 to 4 as below

  1. = no palpable goitre
  2. = Palpable goiter but invisible
  3. = Goitre only visible to experienced clinician
  4. = Easily visible goitre
12 months
Peri-operative pain scores (0-10)
Tijdsspanne: 12 months
To measure the change in pain score before and after ablation. The pain score is from 0 to 10, the higher score means more painful.
12 months

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

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Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

5 december 2023

Primaire voltooiing (Geschat)

1 november 2026

Studie voltooiing (Geschat)

30 juni 2027

Studieregistratiedata

Eerst ingediend

31 augustus 2026

Eerst ingediend dat voldeed aan de QC-criteria

31 augustus 2026

Eerst geplaatst (Werkelijk)

4 september 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

4 september 2026

Laatste update ingediend die voldeed aan QC-criteria

31 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

ONBESLIST

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

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Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Nee

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