Status:
RECRUITING
Opioid Sparing Effect of an ISP Nerve Block on Post-Op Pain Control in Posterior Cervical Spine Surgery
Lead Sponsor:
Stony Brook University
Conditions:
Pain, Postoperative
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief 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. I...
Detailed Description
The purpose of this research study is to evaluate the opioid-sparing effect of the use of an Inter-semispinalis plane (ISP) block after posterior cervical spine surgery. Posterior cervical fusion (PC...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
February 21 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
February 1 2026
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT06570577
Start Date
February 21 2025
End Date
February 1 2026
Last Update
March 18 2025
Active Locations (1)
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1
Stony Brook University Hospital
Stony Brook, New York, United States, 11794