Skip to content

A Comparative Study on the Efficacy of Thyroid Microwave Ablation Versus Anti-thyroid Drug Therapy for Refractory Graves' Disease

A Comparative Study on the Efficacy of Thyroid Microwave Ablation Versus Anti-thyroid Drug Therapy for Refractory Graves' Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097736
Enrollment
Unknown
Registered
2025-02-25
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Refractory Graves' disease

Interventions

Control group:Control group (anti-hyperthyroidism): 8 weeks of anti-hyperthyroidism drugs and ß receptor blockers to improve the patients thyroid function to a normal FT4 level.
Experimental group:Study group (thyroid microwave ablation therapy): 8 weeks of anti-hyperthyroidism drugs and ß receptor blockers to improve the patients thyroid function to a normal FT4 level.

Sponsors

The Third Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for Graves' disease, including elevated FT4 levels, suppressed TSH levels, positive Trab results, and clinically detectable diffuse goiter; 2.A history of Graves' disease for 3 years, with continued use of antithyroid drugs or at least one recurrence of the disease; 3.Patients who refused surgery or RAI treatment; 4.Patients aged 18 to 65 years.

Exclusion criteria

Exclusion criteria: 1.Poor general condition, such as severe organic diseases involving the heart, liver, kidney, or other systems, or the presence of terminal malignant or wasting diseases; 2.Female patients with plans for pregnancy in the past year or during pregnancy; 3.Retrosternal thyroid or the majority of the thyroid gland located behind the sternum; 4.Unilateral vocal cord dysfunction on laryngoscopy; 5.Severe coagulopathy, neutropenia, or positive ANCA; 6.Malignant exophthalmos; 7.Adolescent patients; 8.Hyperthyroid patients with significant tracheal compression requiring urgent decompression; 9.Patients with psychiatric disorders or those unable to comply with treatment and follow-up; 10.Other conditions deemed inappropriate for participation by the investigator, such as participants who are unlikely to adhere to the protocol or have severe physiological or psychological conditions that may affect the efficacy or safety of the treatment.

Design outcomes

Primary

MeasureTime frame
Remission rate;

Countries

China

Contacts

Public ContactLi Renyuan

The Third Affiliated Hospital of Guangzhou Medical University

hi_ivyli@163.com+86 20 81292120

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026