Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07360587

Thyroid Artery Embolization for the Treatment of Compressive Goiters.

Led by Université de Sherbrooke · Updated on 2026-01-22

20

Participants Needed

1

Research Sites

204 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Very few studies have investigated TAE as a treatment for goiter with compressive symptoms. What is the efficacy and safety of TAE for the treatment of compressive goiters in a population ineligible for or refusing standard therapy? This is a prospective interventional cohort study that will allow us to standardize imaging by improving quality data collection and fellow-up to assess the efficacy of TAE for compressive symptoms of nodular goiters. Not only to corroborate current emerging results but clearly define the expected results for this technique.

CONDITIONS

Official Title

Thyroid Artery Embolization for the Treatment of Compressive Goiters.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with compressive symptoms or significant tracheal or oesophageal compression at risk of causing symptoms attributed to a goiter
  • Ineligible for surgery or ablative treatments or preference for thyroid artery embolization over other treatments
  • TiRADS category 1, 2, 3, or 4
  • Bethesda categories I or III on two different biopsies or Bethesda II on one biopsy
  • Patient at least 18 years old
Not Eligible

You will not qualify if you...

  • Comorbidities that prevent endovascular procedure
  • TiRADS category 5
  • Bethesda categories IV, V, or VI on biopsy
  • Patient refusal to participate
  • Uncontrolled severe hyperthyroidism
  • Minor patient (under 18 years old)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Universitaire de Sherbrooke

Sherbrooke, Quebec, Canada, J1H5H3

Actively Recruiting

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Research Team

L

Laurent Fradet, MD FRCSC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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