Stellate Ganglion Block in Head and Neck Cancer Surgery

Stopped early · Not applicable

Conditions studied: Head and Neck Cancer, Pain, Postoperative

In brief

The purpose of this study is to evaluate and reduce pain and improve quality of life in patients being treated for head and neck cancer with unilateral surgery. In this study, patients will be randomly assigned to receive either pre-operative stellate ganglion block or no pre-operative treatment. Blocks will be placed by a trained anesthesiologist using ultrasound guidance in the preoperative holding area prior to surgery. All patients will receive the same post-operative pain medication regimen with appropriate pain treatment as needed. Patients will be asked to fill out surveys prior to surgery, while in the hospital after surgery, and at each follow-up appointment for up to 24 months.

Key facts

Study ID
NCT03714906
Run by
Augusta University
People needed
22
Starts
2019-03-22
Expected to finish
2022-09-15
Last updated by the study team
2023-08-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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