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Local ablation of benign thyroid nodules: a prospective multicenter study include radiofrequency ablation,microwave ablation and laser ablation

Development of Image guided intelligent microwave ablation instrument

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONRC-13003087
Enrollment
Unknown
Registered
2013-02-20
Start date
2013-02-04
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Thyroid Nodule

Interventions

RFA:Radiofrequency ablation
LA:Laser ablation
MWA:MWA ablation

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: (meet all of the following conditions can be selected) 1. nodule or predominantly (>20%)solid nodule; 2. maximum diameter of the nodule > 2cm; 3. nodules did not undergo other treatments (such as: radioactive iodine therapy, TSH suppressive therapy, ethanol ablation); 4. the pathologic result of 2 times needle aspiration or core needle biopsy is benign; 5. inoperable due to the patient's bad body conditions or refused to surgery; 6. nodules according to one of the following items below: (1) nodules increased significantly (volume increases more than 50% within 1 year,or at least two diameters of the nodule increase over 20% and it more than 2 mm long]); (2) patients with nodules significantly related symptoms (such as: foreign body sensation, neck discomfort or pain); (3) nodules obviously convex affect the appearance and require treatment; (4) ideological concerns of patients too heavy to affect normal life and denial of clinical observation; (5) autonomously functioning nodules caused symptoms of hyperthyroidism.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (excluding comply with any of the following items) 1. the follicular nodules or biopsy suggest the malignancy; 2. the founction of contralateral vocal cord is not abnormal; 3. severe coagulation disorders; 4. severe cardiac or pulmonary disease; 5. refused to participate in this research or refused to sign an informed consent.

Design outcomes

Primary

MeasureTime frame
volume reduction rate;Cosmetic score;Symptom score;vascularity scale;therapeutic success rate (volume);recurrence rate;complication rate;

Secondary

MeasureTime frame
radiology examination;LOS(length of stay);operative time;parameters of in ablation;thyroid function;

Countries

China

Contacts

Public ContactPing Liang, Zhi-gang Cheng
liangping301@hotmail.com+86 01066939530

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026