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Postoperative Pain of Robotic, Endoscopic and Open Lateral Neck Dissection

Postoperative Pain of Robotic, Endoscopic and Open Lateral Neck Dissection

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06803732
Enrollment
600
Registered
2025-01-31
Start date
2024-11-01
Completion date
2027-12-31
Last updated
2026-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Postoperative, Surgery, Thyroid Diseases

Keywords

Lateral neck dissection, Robotic thyroid surgery, Minimally invasive surgery

Brief 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.

Interventions

OTHERObservations 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

Sponsors

Shanghai 6th People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
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

Design outcomes

Primary

MeasureTime frameDescription
degree of painapproximately 4 hours after surgery, on postoperative day 1, postoperative month 1 and postoperative month 3pain 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
Number of participants with recurrent laryngeal nerve injurythrough study completion, an average of 1 yearimpaired vocal cord mobility confirmed by postoperative laryngoscopy
Number of participants with hypoparathyroidismthrough study completion, an average of 1 yeara postoperative parathyroid hormone level of less than 10 pg/ml

Countries

China

Contacts

CONTACTLing Zhan
15821120972@163.com08615821120972
PRINCIPAL_INVESTIGATORLing Zhan, Dr

Shanghai 6th People's Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026