Preoperative embolization of thyroid arteries in a patient with large multinodular goiter and papillary carcinoma.
Helton Estrela Ramos, Milena Braga-Basaria, Calixto Haquin...
https://pubmed.ncbi.nlm.nih.gov/15671777Actively Recruiting
Led by Université de Sherbrooke · Updated on 2026-01-22
20
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating thyroid artery embolization (TAE) as a treatment option for patients with nodular goiters causing compressive symptoms who are ineligible for or refuse standard therapies like surgery or ablative treatments. This prospective interventional cohort study aims to improve data quality and follow-up to better assess the safety and effectiveness of TAE in relieving compression symptoms and reducing thyroid nodule volume. The study addresses a gap in treatment options for this specific patient population. Participants will receive thyroid artery embolization, which involves blocking the blood flow that feeds the thyroid nodule to reduce its size and relieve symptoms. There is no comparison group, as the study focuses on patients who cannot or do not want to undergo surgery. Enrollment is through convenience sampling in outpatient settings, guided by endocrinologists or otolaryngologists. Follow-ups are planned at 1 week, and 3, 6, and 12 months after the procedure. During the study, participants will undergo assessments including thyroid nodule volume measurement and evaluation of compressive symptoms at multiple post-procedure timepoints. Safety will be monitored through adverse event reports on the day of embolization and during follow-ups. Thyroid and parathyroid function tests will be performed at baseline, around 48 hours post-procedure, and at several intervals up to 12 months. Overall, the study involves careful monitoring of both effectiveness and safety over a year.
CONDITIONS
Thyroid Artery Embolization for the Treatment of Compressive Goiters.
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of embolization
Participants undergo thyroid artery embolization to interrupt blood flow to the thyroid nodule using an embolization technique.
1 visit (in-person)
Duration - 12 months
Participants are monitored after treatment to assess changes in thyroid nodule volume, symptoms, and safety including thyroid and parathyroid function tests.
Visits at 48 hours, 1 week, 6 weeks, 3 months, 6 months, and 12 months after embolization
Total: 1 location
1
Centre Hospitalier Universitaire de Sherbrooke
Sherbrooke, Quebec, Canada, J1H5H3
Actively Recruiting
L
Laurent Fradet, MD FRCSC
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Helton Estrela Ramos, Milena Braga-Basaria, Calixto Haquin...
https://pubmed.ncbi.nlm.nih.gov/15671777Maximilian Bonnici, Connor Nevin, SoHyun Boo
https://pubmed.ncbi.nlm.nih.gov/37273723Haipeng Xiao, Wenquan Zhuang, Shenming Wang...
https://pubmed.ncbi.nlm.nih.gov/12161479E V Galkin, B S Grakov, A V Protopopov
https://pubmed.ncbi.nlm.nih.gov/7985368Michael T McDermott
https://pubmed.ncbi.nlm.nih.gov/32252086Hyun Kyung Lim, Jeong Hyun Lee, Eun Ju Ha...
https://pubmed.ncbi.nlm.nih.gov/23096937Shi-Hui Guan, Hui Wang, Deng-Ke Teng
https://pubmed.ncbi.nlm.nih.gov/32369708Enrico Papini, Rinaldo Gugliemi, Claudio Maurizio Pacella
https://pubmed.ncbi.nlm.nih.gov/27504993Bryan R Haugen, Erik K Alexander, Keith C Bible...
https://pubmed.ncbi.nlm.nih.gov/26462967G A Khairy
https://pubmed.ncbi.nlm.nih.gov/15626055