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Clinical Trial Summary

To evaluate the feasibility and safety of gasless transaxillary posterior endoscopic thyroidectomy (Resection of thyroid lobe and isthmus, lymph node dissection in the central area of the affected side) and open radical thyroidectomy (Resection of thyroid lobe and isthmus, lymph node dissection in the central area of the affected side) as the current standard surgical treatment mode in terms of feasibility and safety of radical thyroidectomy.


Clinical Trial Description

Subjects that suffering from papillary thyroid carcinoma will be randomized into Study Group (gasless transaxillary posterior endoscopic thyroidectomy ) or Control Group (conventional open thyroidectomy). Measure the outcomes as following, early complication rate, life quality score, the number of dissected lymph nodes, the volume of residual gland, 3-year recurrence rate, operation duration, hospital stays, hospitalization expense, and inflammatory and immune response. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05545852
Study type Interventional
Source Nanfang Hospital, Southern Medical University
Contact Baihui Sun, Dr.
Phone +8602062787170
Email sunbh_nfyy@163.com
Status Recruiting
Phase N/A
Start date June 1, 2021
Completion date May 31, 2025

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