Local Anesthetics in Cervical Epidural Injection
Clinical Efficacy of Local Anesthetic Agents With Interlaminar Epidural Steroid Injection for Chronic Neck Pain: A Prospective, Observational Study
1 other identifier
observational
60
1 country
1
Brief Summary
This study aims to evaluate the efficacy of local anesthetic drugs in cervical epidural injections for chronic neck pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2022
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 30, 2022
CompletedFirst Submitted
Initial submission to the registry
November 23, 2025
CompletedFirst Posted
Study publicly available on registry
December 4, 2025
CompletedFebruary 18, 2026
February 1, 2026
7 months
November 23, 2025
February 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Numerical Rating Scale (NRS)
severity of pain from 0 to 11
6 months
Neck Disability Index (NDI)
an assessment tool for neck pain
6 months
Study Arms (2)
Group S
Patients who received cervical epidural corticosteroid injection
Group SLA
Patients who received cervical epidural corticosteroid and local anesthetic injection
Eligibility Criteria
Adult patients with chronic neck pain due to cervical intervertebral disc herniation are planned to have a cervical epidural injection due to the pain originating from intervertebral disc herniation.
You may qualify if:
- Patients who were planned to have a cervical epidural injection due to the pain originating from an intervertebral disc herniation
You may not qualify if:
- Patients younger than 18
- Unwilling to participate,
- Pregnant or pregnancy possibility
- Infection or anatomic variations in the region of the procedure
- Allergic to the drugs to be used in the procedure
- Coagulation disorders
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ondokuz Mayıs University Faculty of Medicine
Samsun, Atakum, 55200, Turkey (Türkiye)
Related Publications (1)
Aslan E, Karaduman A, Yakut Y, Aras B, Simsek IE, Yagly N. The cultural adaptation, reliability and validity of neck disability index in patients with neck pain: a Turkish version study. Spine (Phila Pa 1976). 2008 May 15;33(11):E362-5. doi: 10.1097/BRS.0b013e31817144e1.
PMID: 18469684BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Fatih Özkan, Professor
Ondokuz Mayis University Faculty of Medicine
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assistant professor
Study Record Dates
First Submitted
November 23, 2025
First Posted
December 4, 2025
Study Start
January 1, 2022
Primary Completion
July 30, 2022
Study Completion
July 30, 2022
Last Updated
February 18, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
We agree to share participant data if there is a reasonable request from the reviewers or any kind of officials.