RecruitingNot ApplicableNCT06570577

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

The Opioid Sparing Effect of an Inter-semispinalis Plane Block on Postoperative Pain Control in Posterior Cervical Spine Surgery


Sponsor

Stony Brook University

Enrollment

60 participants

Start Date

Feb 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Inter-semispinalis Plane Block and a drug called Opioids for people with pain, postoperative. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 75 Years.

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

PROCEDUREInter-semispinalis Plane Block

A nerve block targeting the dorsal rami of the cervical spinal nerves can help alleviate postoperative incisional pain.

DRUGOpioids

Routine Pain Management


Locations(1)

Stony Brook University Hospital

Stony Brook, New York, United States

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NCT06570577


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