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

2026年8月31日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

25

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Man Him, Matrix Dr. Fung, MBBS
  • 電話番号:+852 2255 4232
  • メール:mmhfung@hku.hk

研究場所

      • Hong Kong、香港
        • 募集
        • Queen Mary Hospital
        • コンタクト:
          • Man Him, Matrix Dr. Fung, MBBS
          • 電話番号:+852-22554232
          • メール:mmhfung@hku.hk

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.
他の名前:
  • MWA
実験的: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.
他の名前:
  • RFA

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Volume reduction rate (VRR) of thyroid nodule at 6 months and 12 months (%)
時間枠: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
時間枠:12 months
To assess any complications from procedure during follow-up period after ablation
12 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Changes in compressive symptom scores (0-100)
時間枠: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)
時間枠: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)
時間枠: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

協力者と研究者

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出版物と役立つリンク

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一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2023年12月5日

一次修了 (推定)

2026年11月1日

研究の完了 (推定)

2027年6月30日

試験登録日

最初に提出

2026年8月31日

QC基準を満たした最初の提出物

2026年8月31日

最初の投稿 (実際)

2026年9月4日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月4日

QC基準を満たした最後の更新が送信されました

2026年8月31日

最終確認日

2026年8月1日

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