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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04046354
Other study ID # KY2018001
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date August 1, 2019
Est. completion date December 31, 2021

Study information

Verified date March 2021
Source Chinese PLA General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compared with traditional treatment methods, ultrasound-guided thermal ablation is more targeted, less invasive and more reliable. The study compared microwave ablation and radiofrequency ablation to evaluate the efficacy and safety in the treatment of benign thyroid nodules with a multicenter data, which will provide a basis for clinical treatment.


Description:

Ultrasound-guided minimally invasive treatment has accurate positioning, higher targeting, no need for general anesthesia, less trauma for patients, and more reliable efficacy.Currently, it mainly includes percutaneous anhydrous ethanol injection, radiofrequency ablation and microwave ablation for the treatment of thyroid nodules.Currently, radiofrequency ablation and microwave ablation are mainly used to treat thyroid nodules. This study was a randomized, parallel, positive control, and non-inferiority multicenter clinical study.Radiofrequency ablation was used as the positive control.Follow-up was conducted at 1, 3, 6 and 12 months after ablation. The primary endpoint was the rate of nodule volume reduction at 12 months after surgery.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 149
Est. completion date December 31, 2021
Est. primary completion date November 19, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Age>18 years and =75 years - The pathological diagnosis was benign thyroid nodules within 6 months - Diameter =2cm, solid > 80%, the number of multiple nodules= 3 - Participate voluntarily and sign the informed consent Exclusion Criteria: - Coagulation mechanism disorder or bleeding tendency - Patients with severe cardiopulmonary insufficiency - Blood pressure cannot be effectively controlled - abnormal liver function - Blood glucose cannot be effectively controlled - Abnormal thyroid function - Allergic history of ultrasound contrast agent - Suspicious lymph node metastasis in the cervical region - Abnormal contralateral vocal cord function - Pregnant and lactating women - Have participated in clinical trials of any drug and/or medical device within 3 months prior to enrollment - The researchers believe that there are any other factors that are not suitable for inclusion or that affect participants' participation in the study. - Patients with inner pacemaker, hearing aid, metal stent, titanium clip, internal (external) steel plate and other metal objects.

Study Design


Intervention

Device:
Ultrasound-guided Percutaneous Microwave Ablation
Ultrasound-guided Percutaneous Microwave Ablation
Ultrasound-guided Percutaneous Radiofrequency Ablation
Ultrasound-guided Percutaneous Radiofrequency Ablation

Locations

Country Name City State
China Chinese PLA General Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Chinese PLA General Hospital

Country where clinical trial is conducted

China, 

References & Publications (3)

Kihara M, Hirokawa M, Masuoka H, Yabuta T, Shindo H, Higashiyama T, Fukushima M, Yamada O, Takamura Y, Ito Y, Kobayashi K, Miya A, Miyauchi A. Evaluation of cytologically benign solitary thyroid nodules by ultrasonography: a retrospective analysis of 1877 cases. Auris Nasus Larynx. 2013 Jun;40(3):308-11. doi: 10.1016/j.anl.2012.09.007. Epub 2012 Oct 24. — View Citation

Rastogi A, Bhadada SK, Bhansali A. Nodular goiter with multiple cystic and solid swellings. Indian J Endocrinol Metab. 2012 Jul;16(4):651-3. doi: 10.4103/2230-8210.98034. — View Citation

Wright AS, Sampson LA, Warner TF, Mahvi DM, Lee FT Jr. Radiofrequency versus microwave ablation in a hepatic porcine model. Radiology. 2005 Jul;236(1):132-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Volume reduction rate of thyroid nodules volume reduction rate,VRR=(Volume before treatment - volume at follow-up)/Volume before treatment up to 12 months.
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