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临床试验/NCT07370675
NCT07370675招募中不适用

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

Christian Grønhøj Larsen1 个研究点 分布在 1 个国家目标入组 165 人开始时间: 2026年1月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
165
试验地点
1
主要终点
Number of participants who undergo surgical intervention or experience disease progression during active surveillance

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
30 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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

研究组 & 干预措施

Active Surveillance

Experimental

Active surveillance with ultrasound and clinical follow-up in a 5 year period

干预措施: Active surveillance (6, 12, 18, 24, 36, 48, 60 months) (Other)

结局指标

主要结局

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

时间窗: From enrollment in to active surveillance to the end of the follow-up programe at 5 years

次要结局

未报告次要终点

研究者

发起方
Christian Grønhøj Larsen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Christian Grønhøj Larsen

Senior registrar, PhD, DMSci, ass. prof.

Rigshospitalet, Denmark

研究点 (1)

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