Clinical trial Recruiting at 1 site Interventional Ages 18 to 75

Reducing opioid use after neck surgery with a nerve block

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

Run by Stony Brook University · NCT06570577 · Data updated 2026-11-12

This study is testing if a special nerve block can help people having neck surgery use less opioids for pain relief compared to standard pain management.

Quick facts

Study typeInterventional
Ages18 Years to 75 Years
SexAll
Enrollment60 (estimated)
SponsorStony Brook University
Academic / other
Locations1 site (Stony Brook, New York)
StatusRecruiting
StartedFebruary 21, 2025
Main results expectedMarch 2027
Study endsMarch 2027
Registry record updatedApril 29, 2026
Trial IDNCT06570577 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals scheduled for posterior cervical spine surgery from C2 to C7.

Probably not a fit

Patients undergoing emergency procedures, those with certain medical conditions, or those requiring complex surgeries may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This research evaluates the effectiveness of an Inter-semispinalis plane (ISP) nerve block in reducing the need for opioids in patients undergoing posterior cervical spine surgery. Participants will receive either the nerve block or standard pain management, allowing researchers to compare pain levels, opioid consumption, and hospital discharge times between the two groups. The ISP block is a minimally invasive procedure that targets specific nerves in the neck to provide pain relief, potentially leading to improved recovery outcomes and reduced opioid-related side effects.

Why it matters

Potential benefit: If successful, this approach could significantly reduce opioid consumption and improve recovery times for patients after neck surgery.

How similar studies have gone: While some studies have shown promise for nerve blocks in pain management, further data on the ISP block's safety and efficacy are still needed.

Who can join: the full rules

Show full inclusion / exclusion 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

Where it's running

  • Stony Brook University Hospital
    Stony Brook, New York, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.