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Clinical Trial Summary

The goal of this study is to assess the efficacy of continuous local anesthetic wound infusion to improve quality of recovery following ablative surgery and neck dissection.


Clinical Trial Description

Bilateral cervical plexus catheters are convenient and safe to place under the direct vision of the surgeons during ablative and neck dissection. The investigators hypothesize that continuous local anesthetic wound infusion to block bilateral cervical plexus will improve quality of recovery following ablative surgery and neck dissection. The primary endpoint is the quality of recovery, which will be assessed using the 15-item quality of recovery questionnaire (QoR-15). Secondary endpoints include numeric pain scale, number and proportion of patients on salvage analgesics, Incidence of phrenic nerve block, Incidence of recurrent laryngeal nerve block, length of post-anesthesia care unit (PACU) stay, length of post-operative hospital stay. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06201039
Study type Interventional
Source Sixth Affiliated Hospital, Sun Yat-sen University
Contact Chen
Phone +8613922106109
Email 153856346@qq.com
Status Not yet recruiting
Phase N/A
Start date March 1, 2024
Completion date December 31, 2025

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