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Recruiting NCT06316895

The Clinical Outcomes and Prediction of Thermal Ablation for Low-risk Papillary Thyroid Carcinoma

Observational Papillary Thyroid Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: thyroid surgery, ultrasound-guided thermal ablation.
Who it may be relevant to
Registry conditions: Papillary Thyroid Cancer. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Clinical Outcomes and Artificial Intelligence Prediction Model of Ultrasound-guided Thermal Ablation for the Treatment of Low-risk Papillary Thyroid Carcinoma

Overview

1. To evaluate the clinical outcomes of ultrasound-guided thermal ablation and thyroid surgery for the treatment of papillary thyroid carcinoma; 2. To develop and validate a artificial intelligence model to predict the outcomes of ultrasound-guided thermal ablation in the treatment of papillary thyroid carcinoma;

Interventions

  • Procedure thyroid surgery
    thyroid lobectomy
  • Procedure ultrasound-guided thermal ablation
    radiofrequency ablation; microwave ablation or laser ablation

Primary outcome measures

  • rate of disease progression [Time frame: more than 5 year]
Secondary outcome measures (2)
  • Rate of complications [Time frame: 1week]
  • Rate of tumor disappearance [Time frame: 2 year]

Eligibility criteria

Inclusion criteria

  • patients age between 18 and 80 year old, both sex
  • papillary thyroid carcinoma confirmed by core-needle biopsy or fine-needle aspiration
  • the largest diameter ≤2.0 cm
  • no clinical or imaging evidences of extrathyroidal extension, lymph node metastasis and distant metastasis on ultrasound, nech and chest CT
  • follow-up period ≥12 months,

Exclusion criteria

  • patients with convincing evidence of aggressive papillary thyroid carcinoma or other type of thyroid cancer by biopsy
  • history of neck radiation
  • history of thyroid surgery
  • coagulation disorder
  • serious heart, respiratory, liver, or renal failure
  • dysfunction of the vocal cord on the opposite side

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Chinese PLA General Hospital — Beijing

Identifiers

NCT: NCT06316895 · S2023-706

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗