HIFU Reapplication in Benign Nodules
Primary Purpose
Thyroid Nodule
Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Echopulse
Sponsored by
About this trial
This is an interventional treatment trial for Thyroid Nodule focused on measuring HIFU, thyroid nodule, Benign, Reapplication
Eligibility Criteria
Inclusion Criteria:
- patients age older than 18 years,
- a nodule that has previously been completely treated by single-session HIFU ablation but has not responded adequately (i.e. <50% volume reduction from baseline after 6 months),
- a benign nodule without signs of malignancy (e.g, nonsuspicious clinical and US appearance, benign results at cytologic examination performed in the last 6 months, normal serum calcitonin level),
- a nodule measuring on US greater than or equal to 10 mm in three orthogonal dimensions,
- less than 30% of the targeted nodule comprising cystic area,
- HIFU accessibility of the targeted nodule (distance between the skin and the anterior surface of the nodule less than 17 mm, with no interference of the collarbone with HIFU unit movements)
- normal thyrotropin concentration and
- absence of vocal cord immobility at laryngoscopy.
Exclusion Criteria:
- head and/or neck disease preventing hyperextension of the neck,
- history of thyroid cancer or other malignant tumors in the neck region,
- history of neck irradiation,
- intranodular macrocalcifications inducing a shadow substantial enough to preclude treatment with HIFU,
- nodules next to the posterior margin of the thyroid lobe with anteroposterior diameter less than 15 mm,
- pregnancy or lactation,
- any contraindication related to intravenous moderate sedation in the first HIFU treatment.
Sites / Locations
- Queen Mary Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
High Intensity Focused Ultrasound
Arm Description
Outcomes
Primary Outcome Measures
Change in thyroid nodule volume (mL)
To measure the change in volume (mL) of the index (or treated) thyroid nodule 6 months following HIFU reapplication
Secondary Outcome Measures
The efficacy of reapplication HIFU after the first single session in 6 months
To compare the change in volume (mL) of the treated thyroid nodule between the first single session and the reapplication.
The safety of reapplication HIFU after the first single session in 6 months
To assess the safety of reapplication HIFU by recording any complications after the treatment
The rate of vocal cord palsy in reapplication HIFU after the first single session in 6 months
To examine the rate of vocal cord palsy in reapplication HIFU after the first single session in 6 month
The cosmetic score (in 0-10) of reapplication HIFU after the first single session in 6 months
To evaluate the cosmetic score (in 0-10) of reapplication HIFU after the first single session in 6 months
The pain score (in 0-10) of reapplication HIFU after the first single session in 6 months
To evaluate the pain score (in 0-10) of reapplication HIFU after the first single session in 6 month
The satisfactory (in 0-10) of reapplication HIFU after the first single session in 6 month
The satisfactory level, from scoring in 0-10, to examine how participants' satisfaction in the reapplication HIFU after the first single session in 6 months
Full Information
NCT ID
NCT03331172
First Posted
October 27, 2017
Last Updated
October 9, 2018
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT03331172
Brief Title
HIFU Reapplication in Benign Nodules
Official Title
Efficacy and Safety of High Intensity Focused Ultrasound (HIFU) Reapplication in Benign Thyroid Nodules That Had Less-than Adequate Shrinkage Following Single-session HIFU Treatment.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
July 1, 2017 (Actual)
Primary Completion Date
June 30, 2018 (Actual)
Study Completion Date
August 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
High Intensity Focused Ultrasound (HIFU) is a new approach in treating benign thyroid nodule without surgery. It is proven effective and safe relative to traditional surgery. From previous HIFU studies, it caused shrinkage of thyroid nodule up to 70% from original size. Unfortunately, 5-10% of nodule do not shrink. Those which do not shrink are usually large in size and therefore a second HIFU treatment may help. This study is going to evaluate the efficacy and safety of reapplication HIFU after the first single HIFU session in 6 months.
The study will be carried out in the following steps:
Recruit subject from the clinic according to the study criteria.
Arrange the reapplication HIFU treatment within 3 months.
Arrange 4 visits after the HIFU treatment in Post 7 days, Post 1 month, Post 3 months, and Post 6 months; Data collection will be in these 4 visits through the questionnaire or interview by research assistant
The subjects will have further health management with the same team after the study.
Detailed Description
Thyroid nodules are common and although most are benign and remain relatively static in size, some can grow and become large and cause local symptoms over time. In such scenario, thyroidectomy is usually indicated. However, surgery is not only associated with complications but also with high cost and general anesthesia. As a result, there has been a growing interest in exploring less invasive, non-surgical technique for benign thyroid nodules. For solid or predominantly-solid (<30% cystic areas) thyroid nodules, thermal ablation techniques have been shown to be highly effective in causing nodule shrinkage and alleviating symptoms in the long-term. To date, numerous thermal ablation techniques have been described and they include radiofrequency ablation (RFA), percutaneous laser ablation (PLA), microwave ablation and more recently, high intensity focused ultrasound (HIFU). HIFU is now considered the least invasive technique as there is no need for needle insertion into the target lesion during treatment. It works by utilizing focused ultrasound energy to generate heat and induce thermal ablation beneath the skin and other tissue layers. Recent studies (including several from our group) have shown that it is effective in not only inducing significant nodule shrinkage but also in alleviating nodule-related symptoms.
However, despite its overall success, approximately 10 - 15% of solid or predominantly solid nodules do not shrink adequately (i.e. <50% shrinkage from baseline in the first 6-12 months). Although the exact reason why some nodules do not respond remains unclear, it is noted that the majority of these less responsive nodules are larger in size / volume and so, a second or reapplication of ablation might be required to cause further shrinkage and improvement in symptoms [11]. However, the role of HIFU reapplication in nodules with less-than-adequate response (<50% at 6 months) remains undefined. As a result, the present study is aimed to the feasibility and safety of HIFU reapplication in nodules with shrinkage <50% of baseline volume 6 months after single-session HIFU treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thyroid Nodule
Keywords
HIFU, thyroid nodule, Benign, Reapplication
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
High Intensity Focused Ultrasound
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Echopulse
Other Intervention Name(s)
High Intensity Focused Ultrasound (HIFU)
Intervention Description
Echopulse is a real-time US-guided High-intensity focused ultrasound (HIFU) system, the HIFU session is a noninvasive procedure that involves application of a focused high-energy ultrasound beam for thermal tissue ablation inside the targeted zone, with minimal effect on the surrounding tissue
Primary Outcome Measure Information:
Title
Change in thyroid nodule volume (mL)
Description
To measure the change in volume (mL) of the index (or treated) thyroid nodule 6 months following HIFU reapplication
Time Frame
6 months
Secondary Outcome Measure Information:
Title
The efficacy of reapplication HIFU after the first single session in 6 months
Description
To compare the change in volume (mL) of the treated thyroid nodule between the first single session and the reapplication.
Time Frame
6 months
Title
The safety of reapplication HIFU after the first single session in 6 months
Description
To assess the safety of reapplication HIFU by recording any complications after the treatment
Time Frame
6 months
Title
The rate of vocal cord palsy in reapplication HIFU after the first single session in 6 months
Description
To examine the rate of vocal cord palsy in reapplication HIFU after the first single session in 6 month
Time Frame
6 months
Title
The cosmetic score (in 0-10) of reapplication HIFU after the first single session in 6 months
Description
To evaluate the cosmetic score (in 0-10) of reapplication HIFU after the first single session in 6 months
Time Frame
6 months
Title
The pain score (in 0-10) of reapplication HIFU after the first single session in 6 months
Description
To evaluate the pain score (in 0-10) of reapplication HIFU after the first single session in 6 month
Time Frame
6 months
Title
The satisfactory (in 0-10) of reapplication HIFU after the first single session in 6 month
Description
The satisfactory level, from scoring in 0-10, to examine how participants' satisfaction in the reapplication HIFU after the first single session in 6 months
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients age older than 18 years,
a nodule that has previously been completely treated by single-session HIFU ablation but has not responded adequately (i.e. <50% volume reduction from baseline after 6 months),
a benign nodule without signs of malignancy (e.g, nonsuspicious clinical and US appearance, benign results at cytologic examination performed in the last 6 months, normal serum calcitonin level),
a nodule measuring on US greater than or equal to 10 mm in three orthogonal dimensions,
less than 30% of the targeted nodule comprising cystic area,
HIFU accessibility of the targeted nodule (distance between the skin and the anterior surface of the nodule less than 17 mm, with no interference of the collarbone with HIFU unit movements)
normal thyrotropin concentration and
absence of vocal cord immobility at laryngoscopy.
Exclusion Criteria:
head and/or neck disease preventing hyperextension of the neck,
history of thyroid cancer or other malignant tumors in the neck region,
history of neck irradiation,
intranodular macrocalcifications inducing a shadow substantial enough to preclude treatment with HIFU,
nodules next to the posterior margin of the thyroid lobe with anteroposterior diameter less than 15 mm,
pregnancy or lactation,
any contraindication related to intravenous moderate sedation in the first HIFU treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hung Hin, Brian Lang, MBBS (Hons)
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Mary Hospital
City
Hong Kong
Country
Hong Kong
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
27167915
Citation
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HIFU Reapplication in Benign Nodules
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