RecruitingPhase 4ACTRN12619000028101

Does bilateral superficial cervical plexus block improve the quality of recovery after anterior cervical spine surgery?

Does bilateral cervical plexus block improve the quality of recovery for patients undergoing anterior cervical spine surgery: a randomised placebo-controlled trial


Sponsor

Macquarie University

Enrollment

136 participants

Start Date

Oct 21, 2019

Study Type

Interventional

Conditions

Summary

The anterior approach to the cervical spine is a common procedure in spine surgery. There is increased interest in decreasing the length of stay in hospital after this procedure. In addition, there is increased focus on improving the patients experience after surgery. Ultrasound guided bilateral superficial cervical plexus block has been shown to be beneficial in thryoid surgery, but there is a paucity of data related to anterior cervical spine surgery. Therefore, we designed a placebo controlled trial to assess the benefits of this procedure in regards to improving the patients recovery from surgery and decreasing their length of hospital stay.


Eligibility

Sex: Both males and femalesMin Age: 16 Yearss

Plain Language Summary

Simplified for easier understanding

Surgery on the front of the neck to treat cervical spine (neck) problems — such as a slipped disc or spinal instability — is increasingly common. Recovering from this surgery can involve significant pain, which can slow down discharge from hospital. This study investigates whether a nerve block technique called a bilateral superficial cervical plexus block — where local anaesthetic is injected around the nerves in the neck using ultrasound guidance — can improve pain control after surgery and help patients recover faster and go home sooner. This same nerve block has been shown to work well in thyroid surgery, but there is little evidence yet for cervical spine operations. Participants are randomly assigned to receive either the real nerve block or a placebo (inactive) injection, and neither they nor their doctors know which they received. You may be eligible if you are aged 16 or older and are scheduled for anterior cervical discectomy and fusion, anterior cervical disc replacement surgery, or anterior fusion for an isolated cervical spine injury. You are not eligible if you are having surgery for cancer, have multiple trauma injuries, are pregnant, or have allergies to the local anaesthetics used (ropivacaine or bupivacaine).

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Immediately following induction of anaesthesia and intubation, bilateral ultrasound guided superficial cervical plexus blocks will be placed by an anaesthetist experienced in delivering the block. Pa

Immediately following induction of anaesthesia and intubation, bilateral ultrasound guided superficial cervical plexus blocks will be placed by an anaesthetist experienced in delivering the block. Patients randomised to the local anaesthetic group will receive 15mL of 0.2% ropivacaine on each side (totalling 30mLs).


Locations(3)

Macquarie University Hospital - Macquarie Park

NSW, Australia

Nepean Hospital - Kingswood

NSW, Australia

Nepean Private Hospital - Kingswood

NSW, Australia

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ACTRN12619000028101