ClinicalTrials.gg
RecruitingNCT07906821Updated Nov 2, 2026

Ultrasound-guided Microwave Ablation of Benign Thyroid Nodules

An interventional study of ultrasound-guided percutaneous microwave ablation (MWA) in Thyroid Nodule (Diagnosis), sponsored by Chinese University of Hong Kong. Recruiting at 1 site in Hong Kong. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-02.

Sponsored by Chinese University of Hong Kong · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 1 month after the study started (first participant enrolled Aug 2023, registered Oct 2026).
  • Started Aug 2023; still recruiting 3 years 2 months later.
Updated Oct 30, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to learn if microwave ablation of benign thyroid nodules under local anaesthesia is a safe and effective procedure compared to open thyroidectomy.

The main questions it aims to answer are:

Dose microwave Ablation effectively cause shrinkage of thyroid nodules? Can ablation of selective area of nodules be safely performed under ultrasound guidance, avoiding critical structures including recurrent laryngeal nerve, major vessels and trachea? Researchers will recruit subjects with symptomatic benign thyroid nodules for Microwave Ablation.

Participants will:

Undergo ultrasound guided Microwave Ablation of benign thyroid nodules. Visit the clinic at post operation 2-week, 3-month, 6-month, 12-month, 2-year and 3-year for checkups and tests.

Fill in questionnaire at each clinic visit for pain, pressure symptoms, cosmetic overall satisfaction in Visual Analog Scale.

Read the detailed description

Benign thyroid nodules are common in the general population. Some of them can cause significant patient concerns including compression symptoms and cosmetic issues. Traditional treatment of symptomatic benign thyroid nodules has been surgical excision which is a procedure under general anaesthesia and carries peri-operative complications. Microwave ablation (MWA) is a minimally invasive procedure, which is used for benign and malignant tumors of liver and lung. It has gained attention among otolaryngologists as it could be a minimally invasive procedure under local anaesthesia and effectively causes shrinkage of thyroid nodules, according to some recent studies. Ablation of selective area of nodules can be safely performed under ultrasound guidance, avoiding critical structures including recurrent laryngeal nerve, major vessels and trachea. Effect of ablation could also be 'visualized' real time with ultrasound images.

This is a prospective study. There is one arm, Microwave Ablation of thyroid nodules. We will recruit 60 subjects with symptomatic benign thyroid nodules for Microwave Ablation.

Under ultrasound guidance, the microwave electrode was inserted targeted to the nodule. The extent of the ablated zone is determined real-time by the echogenic changes around the electrode. Ablation will be away from important structure, including major vessels, recurrent laryngeal nerve and trachea.

Participants will have clinic visit at post operation 2-week 3-month, 6-month, 12-month, 2-year and 3-year for checkups and tests.

02

Conditions studied

  • Thyroid Nodule (Diagnosis)

Keywords

  • Microwave ablation
03

In context

Thyroid Nodule

207 studies on the registry are indexed under Thyroid Nodule; 64 are open to participants now.

This study's planned enrollment of 60 is below the median of 75 across 121 interventional studies indexed under Thyroid Nodule.

Browse Thyroid Nodule studies →

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,454 studies on the registry; 474 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Thyroid nodules or dominant nodule of multinodular goitre
  • Symptomatic thyroid nodule not less than 2cm
  • Benign thyroid nodule confirmed by Fine needle aspiration for cytology (FNAC)

Exclusion criteria

Exclusion Criteria:

  • Asymptomatic thyroid nodule
  • Malignant thyroid nodule
  • High risk USG features or cytological features
  • Previous anterior neck surgery
  • Previous radiotherapy at the head and neck region
  • Presence of another , lateral neck, or distant
  • Cervical spine disease precluding extension of the neck
  • Patients under 18 years old
  • Vulnerable population (e.g. Cognitive impairment, pregnancy)
  • Obesity with > 35kg/m2
  • Severe concomitant illness that drastically shortens or increases risk of therapeutic intervention
  • Non-correctable coagulopathy
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Microwave Ablation

    Microwave ablation (MWA) is a minimally invasive, image-guided medical procedure that used to shrink benign (non-cancerous) thyroid nodules

    Procedure: ultrasound-guided percutaneous microwave ablation (MWA)

Interventions

  • Procedureultrasound-guided percutaneous microwave ablation (MWA)

    Under ultrasound guidance, the microwave electrode was inserted targeted to the nodule. Ablation is carried out one axial plane at a time, from inferior to superior aspect of the targeted lesion. Within each axial plane, ablation is performed from deep to superficial manner to prevent bubble generated by the ablation from hindering ultrasound examination. The extent of the ablated zone is determined real-time by the echogenic changes around the electrode. Ablation will be away from important structure, including major vessels, recurrent laryngeal nerve and trachea. During the procedure, the patient's vital signs including O2 saturation, blood pressure and heart rate would be monitored. Operative procedures, difficulties encountered (if any) and operation time will be documented.

06

What researchers measure

Primary outcomes

  1. Thyroid nodule volume reduction rate (VRR) at 3 months post operation

    Thyroid nodule volume is measured via ultrasound and calculated using the ellipsoid formula (length × width × depth × π/6). Changes in nodule volume are expressed as the VRR (%) calculated using the following formula: (Baseline volume - nodule volume at 3 months post operation) × 100/ Baseline volume. This is the percentage measurement of how much a nodule has shrunk compared to its size before the procedure. A positive thyroid nodule volume reduction rate (VRR) means that the physical size (volume) of a thyroid nodule has successfully decreased following the operation. A negative thyroid nodule volume reduction rate (VRR) means that the size or volume of a thyroid nodule increased rather than shrank after a monitoring period.

    Time frame: Baseline and 3 months post operation

Secondary outcomes

  1. Procedure time of microwave ablation

    Procedure time is defined as the duration from the insertion of the microwave ablation antenna into the patient until the removal of the antenna, measured in minutes.

    Time frame: At the time of operation (Day 0)

  2. Pain intensity as assessed by the Visual Analog Scale (VAS)

    The Visual Analog Scale (VAS) is a self-reported instrument used to measure subjective pain intensity after the operation. The total score ranges from 0 to 10, where a score of 0 represents "no pain" and a score of 10 represents "the worst imaginable pain". Higher scores indicate greater pain severity. Maximum pain score recorded on the day of the microwave ablation procedure (Day 0)

    Time frame: Day 0

  3. Overall Satisfaction Score of the operation at 3 years post operation

    Overall satisfaction of the operation assessed using a Visual Analog Scale (VAS). Scores range from 0 to 10, where 0 indicates "completely dissatisfied" and 10 indicates "completely satisfied". A higher score represents a better outcome.

    Time frame: 3 years post operation

  4. Change From Baseline in Visual Analog Scale (VAS) Score for Pressure Symptoms at 3 years post operation

    The Visual Analog Scale (VAS) is used to self-report the severity of pressure symptoms. The scale ranges from 0 to 10, where 0 indicates "no symptoms" and 10 indicates "the most severe symptoms imaginable". Higher scores represent worse outcomes.

    Time frame: Baseline and 3 years post operation

07

Study locations

1 of 1 sites recruiting
  • The Chines University of Hong Kong
    Shatin, Hong Kong
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 30, 2026
Show all 2 updates
  1. Nov 2, 2026
    Minor edits only
    + 1 other change: arm descriptions
  2. Oct 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07906821
Responsible party
Samuel Chung Chie Cheng (Associate Consultant, Chinese University of Hong Kong) — Principal investigator
First posted
Oct 30, 2026
Start date
Aug 31, 2023
Primary completion
May 31, 2029 (estimated)
Completion
May 31, 2029 (estimated)
Last update
Nov 2, 2026

Study contacts

Samuel Chung Chie Cheng
Contact
ccc353@ha.org.hk
852 + 95173435
Cherrie Ng
Contact
cherrieng@cuhk.edu.hk
852 + 35051409
Samuel Chung Chie Cheng
principal investigator · Chinese University of Hong Kong

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion