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NCT07776262Recruiting

Safety and Efficacy of Cryoablation for Thyroid Tumors

Study on the Safety and Efficacy of Cryoablation Therapy for Thyroid Tumors

Source: ClinicalTrials.gov · Last updated 20 Aug 2026

Brief summary (registry, in English)

The goal of this clinical study is to learn if cryoablation works to treat thyroid tumors. It will also learn about the safety of cryoablation for thyroid tumors. The main questions it aims to answer are: * Does cryoablation shrink thyroid tumors over time? * What side effects or problems do participants have after cryoablation? Participants will receive cryoablation treatment guided by ultrasound. Researchers will track tumor size changes and check for any safety issues during follow-up visits.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
108 (estimated)
First submitted
13 Aug 2026
Start date
9 Feb 2026
Primary completion date
10 Jan 2030
Lead sponsor
Yukun Luo
NCT number
NCT07776262

What you commit to

  • Study type: Interventional
  • Planned participants: 108
  • From 9 Feb 2026 to the primary completion date, 10 Jan 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • (1) Biopsy confirms high-risk subtype papillary thyroid carcinoma; (2) History of thyroid surgery or radiotherapy; (3) Complicated with malignant tumors in other sites; (4) Severe coagulation dysfunction, or patients taking oral anticoagulants who have not reached the required drug-withdrawal period; (5) Incomplete follow-up data. 【Group 2: Benign thyroid nodule patients】
    • Patients with uncorrected psychiatric disorders or consciousness disturbance who cannot cooperate with treatment;
    • Patients with neck extension disorders of various causes who cannot cooperate with treatment;
    • Severe coagulation dysfunction, or patients taking oral anticoagulants who have not completed the required drug withdrawal period;
    • Severe cardiopulmonary insufficiency and inability to lie supine for the procedure;
    • Unrecovered recurrent laryngeal nerve injury contralateral to the lesion.

Other

  • 【Group 1: Papillary Thyroid Carcinoma (PTC) patients】

Who the study is looking for

  • 【Group 1: Papillary Thyroid Carcinoma (PTC) patients】
  • Pre-operative ultrasound evaluation shows the maximum tumor diameter \<1 cm;
  • Papillary thyroid carcinoma (PTC) confirmed by ultrasound-guided fine-needle aspiration (FNA) biopsy;
  • Solitary PTC confirmed by pre-operative ultrasound;
  • Imaging examinations demonstrate no extrathyroidal invasion, cervical lymph node metastasis or distant metastasis.
    • 【Group 2: Benign thyroid nodule patients】
  • Benign nodule confirmed by puncture biopsy;
  • Preoperative ultrasound confirms solid nodule with maximum diameter greater than 2 cm;
  • Patients refuse surgical treatment or cannot tolerate surgery, voluntarily receive thyroid ablation therapy and sign the informed consent form.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chinese People's Liberation Army General Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.