The Effectiveness of Thoracal Epidural Steroid and Local Anesthetic Injection
CompletedNot applicableNCT06507995
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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
- Conditions
- Chronic Postoperative Pain
- Chest Pain
- Back Pain
- 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