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

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary and study completion dates: Feb 2026 to Mar 2027v5
  2. Trial status: Not Yet Recruiting to Recruitingv4 Show 6 more changesShow less
    • Start date changed from estimate of Oct 2024 to Feb 21, 2025
    • Primary and study completion dates: Sep 2025 to Feb 2026
    • Eligibility criteria shortened, about 69 words
    • Site details revised
    • Study title revised
    • Study description shortened, about 1 word
  3. Start date: Aug 2024 to Oct 2024
    • Trial status: Recruiting to Not Yet Recruiting
    • Primary and study completion dates: Aug 2025 to Sep 2025
    • Site details revised
    v3
  4. Secondary endpoints: details revised at 1 of 4 entriesv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06570577
Lead Sponsor Stony Brook University
Conditions
(from sponsor)		 Pain, Postoperative
Related terms Klippel-Feil Syndrome, Postoperative Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov