Skip to content

The Effectiveness of Thoracal Epidural Steroid and Local Anesthetic Injection

CompletedNot applicableNCT06507995
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The primary objective was to evaluate the effectiveness of thoracic interlaminar epidural injections in alleviating pain and enhancing function in patients suffering from chronic mid and/or upper back pain. Materials and Methods One hundred patients were randomly divided into two groups, each consisting of 50 patients. Group I received only a local anesthetic, while Group II received a combination of local anesthetic and steroids. The random assignment to either Group I or Group II was determined using a simple computer-generated sequence. Outcomes were evaluated using the Numeric Rating Scale (NRS) and the revised Oswestry Disability Index (rODI). Patients who showed significant improvement for more than four weeks after the first two procedures were deemed successful. Those who did not were classified as failed participants. Significant improvement was defined as a reduction of more than 50% in both NRS and rODI scores, with assessments conducted at baseline and at 3, 6, and 12 months post-treatment. The center where the study was conducted: Ankara University, Faculty of Medicine, Department of Anesthesiology and Reanimation, Division of Algology, Ankara, Turkey

Study details

Official title
The Effectiveness of Thoracal Epidural Steroid and Local Anesthetic Injection
Interventions
  • Drug: thoracic interlaminar epidural injection
Sponsor
Ankara University
Start date
2021-08-15
Primary completion
2023-12-30
Sex
All
Age range
from 18 Years to 86 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
Turkey (Türkiye)
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * \> 18 years old * \> 6 months pain duration * Failed conservative management (including medication, physical therapy, and exercise programs) * Facet joint pain ruled out (confirmed through diagnostic blocks) Exclusion Criteria: * \< 18 years old * Having a psychological illness * Allergies to local anesthetics or steroids * Thoracic facet joint pain * Significant disc herniation * Infection ( which were ruled out by pre-procedure blood tests and C-reactive protein levels)

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06507995