Active Surveillance for Bethesda IV Thyroid Nodules

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30+
SponsorChristian Grønhøj Larsen

About this trial

The traditional surgical approach for Bethesda IV thyroid nodules burdens healthcare systems and patients with costs, perioperative morbidity, and potential long-term consequences of hemithyroidectomy, including hypothyroidism (requiring lifelong thyroid hormone replacement), nerve damage, infection, voice discomfort and postoperative bleeding. Moreover, patient-reported anxiety and reduced quality of life often follow surgery, regardless of benign final pathology. Conversely, surveillance strategies that include periodic ultrasound assessment, clinical examination, and patient education may reduce overtreatment, preserve thyroid function, and optimize resource utilization.

This prospective cohort protocol seeks to address these gaps by systematically evaluating the safety, feasibility, patient experience, and clinicopathologic predictors of progression for Bethesda IV nodules \<2 cm managed with active surveillance.

Our hypothesis is: In patients with thyroid nodules smaller than 2 cm and cytology consistent with Bethesda IV, active surveillance is a safe and feasible alternative to immediate surgery. We hypothesize that only a minority of patients will demonstrate clinically significant tumor progression or require surgical intervention within five years, and that prospective surveillance can prevent unnecessary thyroid operations without compromising patient safety or long-term outcomes.

The primary aim of this study is to determine the proportion of patients with Bethesda IV thyroid nodules \<2 cm who undergo surgical intervention or experience disease progression over a 1-, 2- and 5 year AS period.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

age of 30 years or older AND

a single nodule with a Follicular neoplasm or suspicious for a follicular neoplasm (category IV in the Bethesda system) AND

tumor size of less than 2 cm in all dimensions AND

EU-TIRADS 3 or 4 in Ultrasound imaging examination.

Disqualifiers

EU-TIRADS 5 in Ultrasound imaging examination.

suspicion of disseminated disease because of PET-positive lymph nodes; suspect lymph-nodes by US or by CT-scan; or signs of capsular invasion of the tumor, or irregular shape or margins, extrathyroidal growth OR

tumor placement at a high-risk location (in the thyroid capsule with extracapsular extension toward vessels, RLN, or the trachea) OR

previous thyroid surgery OR

Trial design

Design model

Single group

Treatments tested in this trial

  • Active surveillance (6, 12, 18, 24, 36, 48, 60 months)

    Other intervention

    Active Surveillance og thyroid nodules with Bethesda IV cytology instead of surgery (diagnostic hemithyroidectomy).

Treatment groups

165 Participants
are divided into 1 treatment group
Group A: Active SurveillanceExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Number of participants who undergo surgical intervention or experience disease progression during active surveillance

Time frame
From enrollment in to active surveillance to the end of the follow-up programe at 5 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Christian Grønhøj Larsen

Lead sponsor

Rigshospitalet, Denmark

Sponsor institution

Rigshospitalet, Denmark

Collaborator