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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 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 108 other Pain, Postoperative trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.

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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.

Conditions Studied

Pain, Postoperative

Interventions

  • PROCEDURE Inter-semispinalis Plane Block
  • DRUG Opioids

Study Locations (1)

New York

  • Stony Brook University Hospital - Stony Brook

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2025-02-21
Est. Completion 2026-02
Phase NA

Sponsor

Stony Brook University

127 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06570577

The ClinicalTrials.gov registry entry for NCT06570577 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (78% lower). The listed sponsor is Stony Brook University, which has 127 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

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Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.