Observations on clinicopathological factors influencing the assessment score of surgery
Observations on clinicopathological factors influencing the assessment score of surgery: Age, body mass index, gender, thyroid function parameters, lesion size, lesion location, ultrasound data
Study summary
To develop and validate a structured scoring tool (robotic thyroidectomy assessment score, RTAS) for assessing and quantifying surgical performance in robotic thyroidectomy (RT).
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Clinical diagnosis of differentiated thyroid cancer with a maximum diameter not exceeding 4 cm
* Clinical diagnosis of benign thyroid nodules with a maximum diameter not exceeding 6 cm
* Participants with high cosmetic expectations
* Participants underwent robotic thyroidectomy without open conversion
Exclusion Criteria:
* Participants with history of neck surgery or radiation
* Participants with vocal fold fixation by preoperative fibrolaryngoscope
* Participants with preoperative examination suggestive of distant invasion
* Participants with fusion or fixed of lymph nodes in the neck
Primary outcome measure(s)
Number of participants with recurrent laryngeal nerve injury — through study completion, an average of 1 year impaired vocal cord mobility confirmed by postoperative laryngoscopy
Number of participants with hypoparathyroidism — through study completion, an average of 1 year a postoperative parathyroid hormone level of less than 10 pg/ml
Operative time — through study completion, an average of 1 year operative time was defined as the duration from incision to closure, and was collected from anesthesia record sheet
Score for surgical competence — at the end of robotic thyroidectomy score evaluated by the proposed assessment system
Trial sites (1)
Facility
City
Region
Status
Shanghai Sixth People's Hospital
Shanghai
China
Recruiting
More Shanghai 6th People's Hospital trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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