Clinical Trial

Percutaneous Thermo-ablation for the Treatment of Benign Thyroid Nodules

Study acronym: BIRRO-TA
Recruiting
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Summary
The goal of this observational study is to learn if radiofrequency ablation (RFA), a minimally invasive thermoablation technique, can safely reduce symptoms and improve quality of life in adults with symptomatic benign thyroid nodules or autonomously functioning thyroid nodules. The main questions it aims to answer are: * Does RFA improve health-related quality of life (HRQoL) as measured by the ThyPRO-39 questionnaire? * Does RFA effectively reduce nodule volume and related symptoms (compressive or cosmetic)? Participants will: * Undergo a radiofrequency ablation procedure of the thyroid nodule performed under ultrasound guidance in an outpatient setting. * Complete quality of life questionnaires (ThyPRO-39) before treatment and at follow-up visits. Attend follow-up visits at 1, 3, 6, and 12 months with: * Ultrasound assessments of the thyroid nodule * Symptom and cosmetic scoring * Blood tests to monitor thyroid function * Safety checks for possible complications
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-11-14.
Status change: Not Yet Recruiting → Recruiting 2026-04-23
Trial Details
NCT Number NCT07237373
Lead Sponsor University Hospital, Ghent
Collaborators: Universitaire Ziekenhuizen KU Leuven, AZ Sint-Jan AV
Conditions Benign Thyroid Nodule
Enrollment 50 participants
Start Date 2026-03-03
Primary Completion 2030-02-28 (estimated)
Study Completion 2031-04-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-29