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Success Rates and Safety of Steroid Injections in Managing Spinal and Sacro-Iliac Pain (CORTisone Injection Spine Study)

NCT ID: NCT07762170
Registry status: Recruiting
Study type: Interventional
Phase: Phase 4
Sponsor: Igor Wilderman. MD
Conditions: Back Pain Lower Back, Failed Back Surgery Syndrome (FBSS), Intervertebral Disc Disorders With Radiculopathy, Lumbar Region, Neck Pain, Radiculopathy Multiple Sites, Sciatica, Spinal Stenosis Cervicothoracic Region, Spinal Stenosis Lumbar, Spine Osteoarthritis

Overview

ClinicalTrials.gov lists this study as Recruiting.

Official title: Success Rates and Safety in Managing Spinal and Sacro-Iliac Pain: A Critical Analysis

Enrollment: 500 participants (Estimated).

What is being studied

Intervention: betamethasone acetate phosphate
Drug: Celestone Soluspan 6Mg/Ml Suspension for Injection
Intervention: Colloids
Intervention: Complex Mixtures
Drug: Depo-Medrol 40Mg/Ml Suspension for Injection
Intervention: Dexamethasone
Drug: Dexamethasone
Intervention: Dosage Forms
Intervention: Drug Administration Routes
Intervention: Drug Therapy
Intervention: Fused-Ring Compounds
Intervention: Injections
Intervention: Methylprednisolone
Intervention: Methylprednisolone Acetate
Intervention: Pharmaceutical Preparations
Intervention: Polycyclic Compounds
Intervention: Prednisolone
Intervention: Pregnadienes
Intervention: Pregnadienetriols
Intervention: Pregnanes
Intervention: Steroids
Intervention: Steroids, Fluorinated
Intervention: Suspensions
Intervention: Therapeutics
Intervention: Triamcinolone
Intervention: Triamcinolone Acetonide
Drug: triamcinolone acetonide (Kenalog)

Who may be eligible

Ages: 18 Years to no maximum
Sex: All
Healthy volunteers accepted: No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * \>18 years of age; * Diagnosis of lumbar, cervical, or thoracic pain with various etiologies; * Eligibility to receive steroid injections for back pain, including epidural, facet joints, or SIJ injections, or other injections (e.g., local anesthetics); * Being willing and able to provide NRS pain ratings and PROMIS functionality ratings before the intervention, and the same scores plus IPR, fIPR, and PGIC at various follow-up points after the intervention; * Provide written informed consent. Exclusion Criteria: * Diagnosis of dementia, Parkinson's disease or other cognitive impairments; * Congenital or acquired polyneuropathy; * Back surgery in the month before injection treatment or planned surgery in the subsequent 3 months; * Any clinically significant acute or chronic medical condition that in the judgment of Investigator may preclude injection in the epidural space or compromise patient safety, limit patient's ability to complete the study, and/or compromise the objectives of the study; * Participation in any other competing clinical study within 3 months prior to screening and during the study period.

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: Canada

Ontario, Canada: 1

Sample of listed locations

Wilderman Medical Clinic — Thornhill, Ontario, L4J 1W3, Canada — Recruiting

Study details

Start date: July 30, 2026
Primary completion date: December 1, 2029
Completion date: March 1, 2030
First posted: August 13, 2026

Source and update information

Source: ClinicalTrials.gov
NCT ID: NCT07762170
Registry last updated: August 13, 2026
QualifiedStudies registry data refreshed: October 5, 2026
QualifiedStudies record fetched: October 5, 2026

View NCT07762170 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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