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NCT06570577 · ClinicalTrials.gov registry record · NA
Opioid Sparing Effect of an ISP Nerve Block on Post-Op Pain Control in Posterior Cervical Spine Surgery
A NA study of Pain, Postoperative, sponsored by Stony Brook University.
- Recruiting
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT06570577: Recruiting NA study of Pain, Postoperative, sponsored by Stony Brook University.
NCT06570577 is a NA study of Pain, Postoperative that is actively recruiting participants, run by Stony Brook University. The registered enrollment target is 60 participants, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06570577, a NA study of Pain, Postoperative, is actively recruiting participants, sponsored by Stony Brook University.
- RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
Comparison of the reduction in Morphine Milligram Equivalent (MME) dose of opioids consumed between the control group versus the nerve block group.
Conditions Studied
Interventions
- PROCEDURE Inter-semispinalis Plane Block
- DRUG Opioids
Study Locations (1)
New York
- Stony Brook University Hospital - Stony Brook
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2025-02-21 |
| Est. Completion | 2026-02 |
| Phase | NA |
What NCT06570577 shows while recruiting
NCT06570577 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (78% lower).
The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Inter-semispinalis Plane Block is the first listed.
NCT06570577 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT06570577 about?
NCT06570577 is a clinical study titled "Opioid Sparing Effect of an ISP Nerve Block on Post-Op Pain Control in Posterior Cervical Spine Surgery". 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...
What is the current status of trial NCT06570577?
This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2025-02-21. Estimated completion is 2026-02.
What conditions does trial NCT06570577 study?
This clinical trial studies the following conditions: Pain, Postoperative.
What interventions are being tested in trial NCT06570577?
The interventions under investigation include: Inter-semispinalis Plane Block (PROCEDURE), Opioids (DRUG).
Who is sponsoring clinical trial NCT06570577?
This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06570577 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Pain, Postoperative
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06570577's enrollment target sits among peer trials
60 79th of 113 higher than 30 of 113 other Pain, Postoperative trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain, Postoperative trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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