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NCT Number: NCT07370675

Active Surveillance for Bethesda IV Thyroid Nodules

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.

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Key information

Age range

30 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Otolaryngology, Head and Neck SurgeryRigshospitalet

Copenhagen, 2100, Denmark

Location status: Recruiting

Location contact

Nicoline Thorup, MD, PhD Fellow

CONTACT

[email protected]

0045 45356863

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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
  • concomitant hyperparathyroidism (ionized calcium > 1.32 mmol/L and PTH > 6 pmol/L) OR
  • if the patient is pregnant OR
  • If the patient is unable to give informed consent. OR
  • If calcitonin is elevated above normal level

Treatment and study plan

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

Other

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

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

Study contacts

Contact information is provided by the study sponsor or research team.

Nicoline Thorup, MD, PhD Fellow

CONTACT

[email protected]

0045 45356863

Sponsors and collaborators

Lead sponsor

Christian Grønhøj Larsen

Other

Collaborators

  • Rigshospitalet, Denmark

Registry information

Official study title

Active Surveillance for Small Thyroid Nodules With Bethesda IV Cytology: A Prospective Cohort Study Protocol

Important dates

Study start
2026
Primary completion
2033
Study completion
2033
First posted
Jan 27, 2026
Registry last updated
Jan 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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