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Study identifier: NCT06570577 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Pain, Postoperative  ·  Sponsor: Stony Brook University

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Eman Nada, MBBCH  ·  516-287-9118  ·  Eman.Nada@stonybrookmedicine.edu

Darcy Halper, B.S.  ·  631-444-2970  ·  Darcy.Halper@stonybrookmedicine.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Stony Brook University HospitalStony Brook, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06570577