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Ultrasound-guided Thermal Ablation for Papillary Thyroid Carcinoma

The Clinical Outcomes of Ultrasound-guided Thermal Ablation for the Treatment of Papillary Thyroid Carcinoma: A Multicenter Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06733740
Enrollment
3000
Registered
2024-12-13
Start date
2024-12-10
Completion date
2030-12-31
Last updated
2025-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Papillary Thyroid Cancer

Brief summary

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

ultrasound-guided thermal ablation to treat tumor

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. patients age between 18 and 80 year old, both sex 2. papillary thyroid carcinoma confirmed by core-needle biopsy or fine-needle aspiration 3. the largest diameter ≤2.0 cm 4. no clinical or imaging evidences of extrathyroidal extension, lymph node metastasis and distant metastasis on ultrasound, neck and chest CT 5. follow-up period ≥12 months

Exclusion criteria

1. patients with convincing evidence of aggressive papillary thyroid carcinoma or other type of thyroid cancer by biopsy 2. history of neck radiation 3. coagulation disorder, serious heart, respiratory, liver, or renal failure 4. dysfunction of the vocal cord on the opposite side

Design outcomes

Primary

MeasureTime frameDescription
rate of disease progressionthrough study completion, an average of 6 monthscervical lymph node metastases, recurrent tumors and persistent tumors confirmed by pathology

Secondary

MeasureTime frameDescription
Rate of complications1 weekcomplications of ablation
Rate of tumor disappearancethrough study completion, an average of 6 monthscomplete disappearance of ablated tumor on ultrasound and contrast-enhanced ultrasound
Rate of volume reductionthrough study completion, an average of 6 monthsvolume reduction of tumor after ablation on ultrasound and contrast-enhanced ultrasound
rate of change of thyroid functionthrough study completion, an average of 6 monthsthyroid function test, including free triiodothyronine, free thyroxine, thyroid stimulating hormone, thyroid peroxidase antibody and anti-thyroglobulin antibodies
rate of delayed surgerythrough study completion, an average of 1 yearpatients underwent surgery after ablation because of anxiety

Countries

China

Contacts

Primary ContactLin Yan, MD
gemma-y@163.com13811237313 ext 86

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026