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

2026년 8월 31일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

25

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Man Him, Matrix Dr. Fung, MBBS
  • 전화번호: +852 2255 4232
  • 이메일: mmhfung@hku.hk

연구 장소

      • Hong Kong, 홍콩
        • 모병
        • Queen Mary Hospital
        • 연락하다:
          • Man Him, Matrix Dr. Fung, MBBS
          • 전화번호: +852-22554232
          • 이메일: mmhfung@hku.hk

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
다른 이름들:
  • MWA
실험적: 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.
다른 이름들:
  • RFA

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Volume reduction rate (VRR) of thyroid nodule at 6 months and 12 months (%)
기간: 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
기간: 12 months
To assess any complications from procedure during follow-up period after ablation
12 months

2차 결과 측정

결과 측정
측정값 설명
기간
Changes in compressive symptom scores (0-100)
기간: 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)
기간: 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)
기간: 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

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여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

간행물 및 유용한 링크

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일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2023년 12월 5일

기본 완료 (추정된)

2026년 11월 1일

연구 완료 (추정된)

2027년 6월 30일

연구 등록 날짜

최초 제출

2026년 8월 31일

QC 기준을 충족하는 최초 제출

2026년 8월 31일

처음 게시됨 (실제)

2026년 9월 4일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 4일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 8월 31일

마지막으로 확인됨

2026년 8월 1일

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