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NCT06666621 · ClinicalTrials.gov registry record · Phase 4

Endogenous Opioid Response to Injections

A Phase 4 study of Low Back Pain and Zygapophyseal Joint Arthritis, sponsored by Middle Tennessee Research Institute.

Recruiting
Registry status
Phase 4
Development phase
33
Enrollment target
1
Study location

NCT06666621: Recruiting Phase 4 study of Low Back Pain and Zygapophyseal Joint Arthritis, sponsored by Middle Tennessee Research Institute.

NCT06666621 is a Phase 4 study of Low Back Pain and Zygapophyseal Joint Arthritis that is actively recruiting participants, run by Middle Tennessee Research Institute. The registered enrollment target is 33 participants, below the 504-participant average among 122 other Low Back Pain trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06666621, a Phase 4 study of Low Back Pain and Zygapophyseal Joint Arthritis, is actively recruiting participants, sponsored by Middle Tennessee Research Institute.

RECRUITING
Registry status
Phase 4
Development phase
33 participants
Enrollment target
1
Study location

Study Summary

This study will study pain relief after spine injections that are used to guide care. Some improvements in pain from a procedure might be from placebo effect rather than the physiological effect of the procedure. The study will use naloxone to reverse the effect of the body's internal placebo system after a spine injection, so the placebo effect and the injection effect can be measured separately. This process may improve the understanding of spine injections and their ability to guide pain care.

Primary Outcome

Endogenous opioid-dependent placebo analgesia is defined as change in analgesia after lumbar medial branch block #1 (measured by numeric pain rating scale) after infusing naloxone

Interventions

  • DRUG Normal saline infusion
  • DRUG Naloxone infusion

Study Locations (1)

Tennessee

  • VA Tennessee Valley Healthcare System - Nashville

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2024-08-22
Est. Completion 2026-02
Phase Phase 4

What NCT06666621 shows while recruiting

NCT06666621 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 504-participant average among 122 other Low Back Pain trials with a reported enrollment target (93% lower).

The record links to 2 conditions, with Low Back Pain appearing as the primary indexed condition, and to 2 interventions - of which Normal saline infusion is the first listed.

NCT06666621 reports a single indexed study location in Tennessee.

Frequently Asked Questions

What is clinical trial NCT06666621 about?

NCT06666621 is a clinical study titled "Endogenous Opioid Response to Injections". This study will study pain relief after spine injections that are used to guide care. Some improvements in pain from a procedure might be from placebo effect rather than the physiological effect of the procedure. The study will use naloxone to reverse the effect of the body's internal placebo system...

What is the current status of trial NCT06666621?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 33 participants. The study started on 2024-08-22. Estimated completion is 2026-02.

What conditions does trial NCT06666621 study?

This clinical trial studies the following conditions: Low Back Pain, Zygapophyseal Joint Arthritis.

What interventions are being tested in trial NCT06666621?

The interventions under investigation include: Normal saline infusion (DRUG), Naloxone infusion (DRUG).

Who is sponsoring clinical trial NCT06666621?

This trial is sponsored by Middle Tennessee Research Institute, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06666621 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Low Back Pain

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 NCT06666621's enrollment target sits among peer trials

33 105th of 122 higher than 18 of 122 other Low Back Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Low Back Pain 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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Source: ClinicalTrials.gov NCT06666621, the US trial registry maintained by the National Library of Medicine. NCT06666621 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.