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Effect of Superficial Cervical Plexus Block on the Postoperative Quality of Recovery

Effect of Superficial Cervical Plexus Block on the Postoperative Quality of Recovery After Anterior Cervical Discectomy and Fusion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01662219
Acronym
QoR
Enrollment
46
Registered
2012-08-10
Start date
2012-08-31
Completion date
2014-06-30
Last updated
2018-02-06

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

Conditions

Cervical Disc Prolapse

Keywords

superficial cervical plexus block, quality of recovery

Brief summary

Pain and discomfort after anterior cervical spine surgery is difficult to quantify and quoted as moderate in severity, often needing oral opioid analgesics. In addition, these patients are more prone for postoperative respiratory complication due to airway edema secondary to surgical retraction or wound hematoma. Opioid analgesics provide good pain control but postoperative nausea and vomiting and respiratory depression are undesirable in these patients who are at risk for postoperative wound hematoma and airway edema The use of multimodal analgesia is rapidly becoming the 'standard of care' for preventing pain after ambulatory procedures at most surgery centers throughout the world . The purpose of this study is to determine whether superficial cervical plexus block will improve the postoperative quality of recovery as measured by Quality of Recovery 40 questionnaire (QoR-40) in patients undergoing elective anterior cervical discectomy and fusion.

Detailed description

Anterior cervical discectomy and fusion is increasingly being done as a day surgery or short stay surgery. Postoperative pain is the leading cause of unplanned hospital admissions following day surgery, a major source of dissatisfaction and often impairs the quality of recovery. Opioid analgesics alone are not always effective and may also worsen the postoperative nausea and vomiting and in turn the postoperative recovery. This study is designed to find out if an injection of freezing on the side of neck around the nerves (superficial cervical plexus block) improves the quality of recovery from anesthesia and surgery by reducing the pain, analgesic consumption after anterior cervical spine surgery. Primary Outcome Measure The primary outcome measure is the global QoR-40 aggregate score at 24 hours after surgery. Secondary Outcome Measures * Postoperative pain scores (first 24 hours) * Total analgesic consumption (first 24 hours) * Time for first opioid administration * Postop Nausea and vomiting (first 24 hours) * Post operative sedation (first 24 hours)

Interventions

OTHERSuperficial cervical plexus block for experimental group

15 ml of 0.25% Bupivacaine will be given for superficial cervical plexus block

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* all adult patients * aged 18-80 years * with ASA class I - III * undergoing anterior cervical disc surgery in supine position

Exclusion criteria

1. In patients who are allergic to local anesthetics 2. ASA- IV patients 3. Lack of informed consent 4. Pregnant patient

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is the global QoR-40 aggregate score after ACDF surgery.24 hours

Secondary

MeasureTime frame
post operative pain score assessment24 hours
Post operative analgesic consumption24 hours
time for the first dose of opioid consumption24 hrs
post operative nausea and vomiting24 hrs
post operative sedation score24 hrs

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026