A Evaluation of High Intensity Focused Ultrasound (HIFU) in the Treatment of Relapsed Graves' Disease (HIFURGD)
Primary Purpose
Rrelapsed Graves' Disease
Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
HIFU Graves
Sponsored by
About this trial
This is an interventional treatment trial for Rrelapsed Graves' Disease focused on measuring HIFU, Graves' disease, treatment
Eligibility Criteria
Inclusion Criteria:
- age older than 18 years;
- relapsed Graves' disease despite an adequate ATD treatment for 18 months or more;
- HIFU accessibility of the targeted area (distance between the skin and the anterior surface of the nodule less than 10 mm; with no interference of the collarbone with HIFU unit movements);
- normal thyrotropin concentration before procedure;
- on at least 2-week of β-blockade prior to HIFU; and
- absence of vocal cord immobility at laryngoscopy.
Exclusion Criteria:
- patients who prefer or indicated for surgery;
- 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;
- severe Grave's ophthalmopathy (GO);
- large compressive goiter;
- pregnancy or lactation; and
- any contraindication related to intravenous moderate sedation.
Sites / Locations
- Queen Mary Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
HIFU Graves
Arm Description
Applying the High intensity Focused Ultrasound treatment to the relapsed Graves' disease Patients.
Outcomes
Primary Outcome Measures
Remission rate of Graves' disease after one successful course of HIFU
To evaluate the remission rate of relapsed Graves' disease after 6 months of HIFU treatment
Secondary Outcome Measures
The pain assessment (scoring 1-10) after treatment
Patient pain score immediately after HIFU treatment.
Incidence of local or general adverse events
The incidence rate of local or general adverse events after completion of HIFU treatment session.
Full Information
NCT ID
NCT02685514
First Posted
February 14, 2016
Last Updated
November 9, 2016
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT02685514
Brief Title
A Evaluation of High Intensity Focused Ultrasound (HIFU) in the Treatment of Relapsed Graves' Disease
Acronym
HIFURGD
Official Title
A Prospective Evaluation of High Intensity Focused Ultrasound (HIFU) in the Treatment of Relapsed Graves' Disease
Study Type
Interventional
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To evaluate the short-term efficiency and safety of HIFU treatment in the relapsed Graves' disease.
Detailed Description
Grave's disease is the most common cause of hyperthyroidism and affects approximately 2% of women and 0.2% of men in the population. The use of antithyroid drugs (ATD) has been the first-line of treatment for Graves' disease in many centers for decades, and its use has been increasing worldwide. One reason for this is that it may induce remission, whereas radioiodine (RAI) and surgery often lead to hypothyroidism and other complications in addition to hospitalization and radiation exposure. However, ATD use is also associated with increasing risk of some adverse minor effects such as skin rash, gastric intolerance, and arthralgia in 5% of patients. Furthermore, major adverse events, such as agranulocytosis and hepatotoxicity may be life-threatening but are rare (<0.5% of cases). These usually occur during the first three to six months of treatment, and tend to be associated with high ATD doses. Therefore, the recommended duration of ATD treatment is generally not longer than 12-24 months. However, despite adequate medical treatment, up to 50-70% of patients with Graves' disease would relapse or recur and therefore, a more definitive approach using RAI treatment or thyroid surgery is eventually needed for the resolution of hyperthyroidism. Although RAI is considered safe and easy to manage, particularly in patients without Grave's ophthalmopathy (GO), subclinical and overt hypothyroidism may occur months or even years after the administration of RAI. Hence, long-term follow-up of thyroid function and GO as well as management of thyroxine replacement is necessary. Similarly, although surgery is the main therapeutic strategy, it carries a 2%-10% risk of complications such as hypocalcemia, transient or permanent recurrent laryngeal nerve palsy, bleeding, or postoperative infection. In view of these, various nonsurgical, minimally invasive treatment alternatives have been developed at specialized treatment centers.
High-intensity focused ultrasound (HIFU) 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. This method has been applied for treatment of a variety of medical conditions such as uterine fibroids and prostate, breast, pancreatic, and liver tumors. A favorable outcome also has been observed in patients with primary or secondary hyperparathyroidism. HIFU has also been proposed for thyroid nodule ablation . In a human feasibility study, 25 patients were treated 2 weeks before a scheduled thyroidectomy. Pathologic analysis demonstrated targeted tissue destruction of 2%-80% without any damage to neighboring structures. To the investigators knowledge, studies of follow-up after HIFU ablation of Graves' disease have not been published, except for one report where two patients received a combination of microwave ablation and RAI. Thus, the purpose of this prospective study is to assess the short-term efficacy and safety of US-guided HIFU ablation for the treatment of relapsed Graves' disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rrelapsed Graves' Disease
Keywords
HIFU, Graves' disease, treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Arm Title
HIFU Graves
Arm Type
Experimental
Arm Description
Applying the High intensity Focused Ultrasound treatment to the relapsed Graves' disease Patients.
Intervention Type
Device
Intervention Name(s)
HIFU Graves
Intervention Description
The HIFU treatment technique will be applied to the recruited participants
Primary Outcome Measure Information:
Title
Remission rate of Graves' disease after one successful course of HIFU
Description
To evaluate the remission rate of relapsed Graves' disease after 6 months of HIFU treatment
Time Frame
6 months
Secondary Outcome Measure Information:
Title
The pain assessment (scoring 1-10) after treatment
Description
Patient pain score immediately after HIFU treatment.
Time Frame
6 months
Title
Incidence of local or general adverse events
Description
The incidence rate of local or general adverse events after completion of HIFU treatment session.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age older than 18 years;
relapsed Graves' disease despite an adequate ATD treatment for 18 months or more;
HIFU accessibility of the targeted area (distance between the skin and the anterior surface of the nodule less than 10 mm; with no interference of the collarbone with HIFU unit movements);
normal thyrotropin concentration before procedure;
on at least 2-week of β-blockade prior to HIFU; and
absence of vocal cord immobility at laryngoscopy.
Exclusion Criteria:
patients who prefer or indicated for surgery;
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;
severe Grave's ophthalmopathy (GO);
large compressive goiter;
pregnancy or lactation; and
any contraindication related to intravenous moderate sedation.
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
ZIP/Postal Code
852
Country
Hong Kong
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
15745981
Citation
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A Evaluation of High Intensity Focused Ultrasound (HIFU) in the Treatment of Relapsed Graves' Disease
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