Menu
Recruiting NCT06803732

Postoperative Pain of Robotic, Endoscopic and Open Lateral Neck Dissection

Observational Pain, Postoperative Thyroid Diseases Surgery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Observations on postoperative pain intensity.
Who it may be relevant to
Registry conditions: Pain, Postoperative, Thyroid Diseases, Surgery. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Interventions

  • Other 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

Primary outcome measures

  • degree of pain [Time frame: approximately 4 hours after surgery, on postoperative day 1, postoperative month 1 and postoperative month 3]
  • Number of participants with recurrent laryngeal nerve injury [Time frame: through study completion, an average of 1 year]
  • Number of participants with hypoparathyroidism [Time frame: through study completion, an average of 1 year]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Shanghai Sixth People's Hospital — Shanghai

Identifiers

NCT: NCT06803732 · 2025-KY-095(K)

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗