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Clinical Trials in Turkey / NCT07787741
Recruiting Not applicable

Cervical Epidural Block in Chronic Neck Pain

NCT07787741 · tracked via the Priya Life Science Turkey tracker
Sponsor
Alİ Eman, MD
Phase
Not applicable
Started
2026-07-01
Last updated
2026-09-08

Condition(s) studied

Chronic Neck PainCervical Radiculopathy

Investigational drug(s) / intervention(s)

Cervical Epidural Steroid InjectionCervical Stabilization Exercise ProgramPhysical Therapy Program

Cervical Epidural Steroid Injection: Participants receive a cervical epidural steroid injection for the treatment of chronic neck pain associated with cervical radiculopathy.

Cervical Stabilization Exercise Program: Participants perform a cervical stabilization exercise program in addition to cervical epidural steroid injection.

Physical Therapy Program: Participants receive a physical therapy program in addition to cervical epidural steroid injection.

Study summary

Chronic neck pain can negatively affect daily activities, work ability, and quality of life. Cervical epidural block is commonly used to reduce pain and inflammation, while exercise and physical therapy aim to improve muscle strength, endurance, movement control, and physical function. However, there is limited evidence comparing cervical epidural block alone with its combined use with exercise or physical therapy.

This study aims to compare the effects of three treatment approaches in patients with chronic neck pain associated with cervical disc pathology or degenerative changes. Participants will receive cervical epidural block alone, cervical epidural block combined with cervical stabilization exercises, or cervical epidural block combined with physical therapy. Pain intensity, neck-related disability, and quality of life will be evaluated before treatment and at 1, 3, and 6 months after treatment using the Numeric Rating Scale, Neck Disability Index, and 12-Item Short Form Health Survey. The study will determine whether adding exercise or physical therapy to cervical epidural block provides additional clinical and functional benefits.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * Aged 18 to 55 years * Neck pain lasting longer than 3 months * Diagnosis of cervical radiculopathy * Numeric Rating Scale (NRS) pain score of 5 or higher Exclusion Criteria: * History of spinal surgery * Cervical spondylolisthesis * Spinal stenosis * Presence of a neurological deficit * History of psychiatric disease * Polyneuropathy * History of spinal fracture * Pregnancy * History of malignancy * Known allergy to any medication used in the study * Central sensitization * Widespread pain * Regional pain associated with a systemic disease

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sakarya Training and Research Hospital Adapazarı Sakarya Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07787741 on ClinicalTrials.gov ↗ ← All trials in Turkey