Opioid Sparing Effect of an ISP Nerve Block on Post-Op Pain Control in Posterior Cervical Spine Surgery
Stony Brook University · NCT06570577
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- February 21, 2025
- Record last updated
- April 29, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Inter-semispinalis Plane Block; Opioids
Conditions: Pain, Postoperative
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Having Posterior Cervical Spine Surgery from C2 - C7, which may extend to the upper thoracic vertebrae, inclusive to T3.
- Capacity to provide informed consent
Exclusion Criteria
- 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.
- The patient is having a complicated surgery or a revision surgery
- Female patient with a positive pregnancy test on the day of surgery (hospital standard-of-care).
- Patient has Diabetes
- Patients who have had a prior adverse reaction to bupivacaine or dexamethasone
- Patients with Glucose-6-phosphate dehydrogenase deficiency or congenital or idiopathic methemoglobinemia
Recruiting US locations
Stony Brook University Hospital
Stony Brook, NY 11794
Site contact: Eman Nada, MBBCH · 516-287-9118 · Eman.Nada@stonybrookmedicine.edu
Study contacts (from the official record)
- Eman Nada, MBBCH · 516-287-9118 · Eman.Nada@stonybrookmedicine.edu
- Darcy Halper, B.S. · 631-444-2970 · Darcy.Halper@stonybrookmedicine.edu
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