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NCT02095197 · ClinicalTrials.gov registry record · Phase 4

C7-T1 Epidural Steroid Injections Versus Targeted Injection for Treatment of Cervical Radicular Pain

A Phase 4 study, sponsored by Northwestern University.

Completed
Registry status
Phase 4
Development phase
79
Enrollment target

NCT02095197 is a Phase 4 study that has completed, run by Northwestern University. The registered enrollment target is 79 participants.

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The verdict

NCT02095197, a Phase 4 study, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
Phase 4
Development phase
79 participants
Enrollment target

Study Summary

Cervical radicular pain is a common, disabling problem, occurs in 83:100,000 individuals per year. Symptoms are most often caused by intervertebral disc herniation (21.9%) or central or foraminal stenosis from spondylosis (68.4%). Patients complain of pain in the head, neck, scapula or arm. The diagnosis of radicular pain is made clinically by history and physical examination, supported by imaging studies and electrodiagnostic tests. No study has compared the differences in pain, medication utilization, functional outcomes, or patient satisfaction between interlaminar and targeted epidural injections in the cervical spine. In theory, the technique of targeted epidural steroid delivery with a catheter has a lower risk of accidental vascular trespass or disc penetration during the procedure, and far less risk of dural penetration or spinal cord injury at rostral levels of the cervical spinal cord as compared with the interlaminar technique. The investigators hypothesize that this technique results in superior pain control, decreased medication use, improved function and fewer repeat injections. This data could improve patient safety and affect the evolving treatment guidelines for cervical epidural injections.

Interventions

  • DRUG Triamcinolone 80mg

Trial Details

FieldValue
Enrollment Target 79 participants
Start Date 2014-03
Est. Completion 2016-07
Phase Phase 4

Sponsor

Northwestern University

1,209 total trials

What the Registry Record Tells You About NCT02095197

The ClinicalTrials.gov registry entry for NCT02095197 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 79 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Triamcinolone 80mg is the first listed.

NCT02095197 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02095197 about?

NCT02095197 is a clinical study titled "C7-T1 Epidural Steroid Injections Versus Targeted Injection for Treatment of Cervical Radicular Pain". Cervical radicular pain is a common, disabling problem, occurs in 83:100,000 individuals per year. Symptoms are most often caused by intervertebral disc herniation (21.9%) or central or foraminal stenosis from spondylosis (68.4%). Patients complain of pain in the head, neck, scapula or arm. The diag...

What is the current status of trial NCT02095197?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 79 participants. The study started on 2014-03. Estimated completion is 2016-07.

What interventions are being tested in trial NCT02095197?

The interventions under investigation include: Triamcinolone 80mg (DRUG).

Who is sponsoring clinical trial NCT02095197?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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.