Opioid Sparing Effect of an ISP Nerve Block on Post-Op Pain Control in Posterior Cervical Spine Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorStony Brook University

About this trial

Participants who have a surgical procedure called Posterior Cervical (neck) Spine Surgery will normally need pain medication to relieve post operative pain. This usually includes opioid medications. In this study, the consented participant may receive a nerve block procedure, in addition to the pain relieving medication. There is a fifty-fifty chance to receive the nerve block. The goal is to see if the nerve block group needs less opioid medication, has lower pain scores and is discharged from the hospital sooner.

Eligibility criteria

Qualifiers

Having Posterior Cervical Spine Surgery from C2 - C7, which may extend to the upper thoracic vertebrae, inclusive to T3.

Capacity to provide informed consent

Disqualifiers

Fusion and decompression due to trauma

Emergent procedures

Patient is on a medication-assisted treatment, e.g., buprenorphine, naltrexone or methadone.

There is an infection near or in the area of neck where the block will be placed.

Trial design

Treatments tested in this trial

  • Inter-semispinalis Plane Block
  • Opioids

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators