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A prospective pilot study of the safety and efficacy of thyroid artery embolisation (TAE) for the treatment of symptomatic thyroid nodular goitre

A prospective pilot study of the safety and efficacy of thyroid artery embolisation (TAE) for the treatment of symptomatic thyroid nodular goitre

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626001049369
Acronym
The TAE Study
Enrollment
5
Registered
2026-08-26
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-08-31

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

Conditions

None listed

Brief summary

The authors aim to perform thyroid artery embolisation (TAE) for a pilot cohort of 5 patients with symptomatic benign thyroid nodules and/or thyroid goitre to determine the safety, feasibility, efficacy and outcomes in the local setting.

Interventions

The intervention is thyroid artery embolisation (TAE), a minimally invasive endovascular procedure used to treat symptomatic thyroid nodular goitre. The procedure is performed by a specialist interventional radiologist with expertise in embolisation techniques. TAE is performed in an interventional radiology suite at The Alfred Hospital and typically takes approximately 60 minutes. Under local anaesthesia, a small catheter is inserted into an artery (typically via the wrist, arm, or groin) and

The intervention is thyroid artery embolisation (TAE), a minimally invasive endovascular procedure used to treat symptomatic thyroid nodular goitre. The procedure is performed by a specialist interventional radiologist with expertise in embolisation techniques. TAE is performed in an interventional radiology suite at The Alfred Hospital and typically takes approximately 60 minutes. Under local anaesthesia, a small catheter is inserted into an artery (typically via the wrist, arm, or groin) and guided to the thyroid arteries under X-ray guidance. Embolic agents, including polyvinyl alcohol (PVA) particles and emolisation coils, are then used to reduce blood flow to the thyroid nodule(s), The procedure is usually performed as a day procedure, with patients observed for a minimum of 4 hours following treatment before discharge, provided they are clinically stable. Follow-up assessments will be conducted by the study investigators at 2 weeks, 6 months, and 12 months following the procedure. Assessments include clinical review, thyroid function tests, imaging (ultrasound and CT), and completion of the ThyPRO-39 questionnaire. Attendance at follow-up visits will be supported through study team coordination and appointment reminders. Fidelity to the intervention will be assessed through adherence to the study protocol, including use of approved embolic materials, documentation of the target vessels treated, embolisation endpoint achieved, procedural details, and completion of scheduled follow-up assessments.

Sponsors

Bayside Health (Alfred Hospital)
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adult patients greater than or equal to 18 years 2. Symptomatic Nodular Thyroid Disease (goitre) 3. Dominant nodule size greater than or equal to 30 cc or dominant nodule with retrosternal extension

Exclusion criteria

1. Thyroid malignancy 2. Iodine contrast allergy 3. Severe renal insufficiency 4. Aberrant arterial anatomy such that embolisation treatment to a sufficient endpoint would be unfeasible 5. Significant atherosclerotic disease such that embolisation treatment to a sufficient endpoint would be unfeasible 6. Severe cardiovascular or respiratory illness 7. Current pregnancy

Outcome results

None listed

Source: ANZCTR · Data processed: Sep 19, 2026