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Clinical Trials in China / NCT06803732
Recruiting Observational

Postoperative Pain of Robotic, Endoscopic and Open Lateral Neck Dissection

NCT06803732 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai 6th People's Hospital
Phase
Observational
Started
2024-11-01
Last updated
2026-06-24

Condition(s) studied

Pain, PostoperativeThyroid DiseasesSurgery

Investigational drug(s) / intervention(s)

Observations on postoperative pain intensity

Observations on postoperative pain intensity: pain intensity was assessed using a standard visual analogue score, with a score of 0 to 10 corresponding to no pain to the most severe pain on operation day, postoperative day 1, postoperative month 1, postoperative month 3

Study summary

Postoperative pain is a good indicator to confirm the advantages of the surgical methods in the era of minimally invasive surgery. Lateral neck dissection requires extensive dissection which may leads to postoperative numbness and pain. Robotic thyroid surgery has the advantage of precise and careful dissection and avoid the L-shape incision in the open approach. The study aims to explore the pain intensity and severity of lateral neck dissection on operation day, postoperative month 1 and postoperative month 3 among the robotic, endoscopic and open approach.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * Patients underwent lateral neck dissection via robotic, endoscopic or open approach * Clinical diagnosis of differentiated thyroid cancer * Clinical diagnosis of metastatic lateral lymph nodes Exclusion Criteria: * Participants with distant metastasis * Participants with history of neck surgery or radiation * Participants with vocal fold fixation by preoperative fibrolaryngoscope

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Sixth People's Hospital Shanghai Shanghai Municipality Recruiting

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Other trials for the same condition

Official registry record

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.

View NCT06803732 on ClinicalTrials.gov ↗ ← All trials in China