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Recruiting NCT06733740

Ultrasound-guided Thermal Ablation for 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: ultrasound-guided thermal ablation.
Who it may be relevant to
Registry conditions: Papillary Thyroid Cancer. Basic parameters: from 18 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 of Ultrasound-guided Thermal Ablation for the Treatment of Papillary Thyroid Carcinoma: A Multicenter Study

Overview

To evaluate long-term outcomes of ultrasound-guided thermal ablation for the treatment of papillary thyroid carcinoma

Detailed description

To evaluate and predict long-term clinical outcomes of ultrasound-guided thermal ablation for the treatment of papillary thyroid carcinoma by a multicenter study

Interventions

  • Procedure ultrasound-guided thermal ablation
    ultrasound-guided thermal ablation to treat tumor

Primary outcome measures

  • rate of disease progression [Time frame: through study completion, an average of 6 months]
Secondary outcome measures (5)
  • Rate of complications [Time frame: 1 week]
  • Rate of tumor disappearance [Time frame: through study completion, an average of 6 months]
  • Rate of volume reduction [Time frame: through study completion, an average of 6 months]
  • rate of change of thyroid function [Time frame: through study completion, an average of 6 months]
  • rate of delayed surgery [Time frame: through study completion, an average of 1 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, neck 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
  • 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: NCT06733740 · 2024-655

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗