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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05340179
Other study ID # 131/10
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 25, 2022
Est. completion date April 30, 2023

Study information

Verified date May 2023
Source Diskapi Teaching and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cervical epidural steroid injections are an accepted treatment modality for radicular pain secondary to disc pathology. With the developing ultrasound technology, ultrasound guided cervical selective nerve root block has been successfully used in the treatment of cervical radiculopathy. We aimed to compare the efficacy of cervical interlaminar epidural injections and cervical selective nerve root block.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date April 30, 2023
Est. primary completion date April 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Cervical radicular pain based on history and physical exam - NRS pain score > 3 Exclusion Criteria: - Previous spine surgery - Allergic reactions to drugs used in procedure - Epidural steroid injection within past 2 years - Radiculopathy not resulting from disc pathology (e.g. foraminal stenosis or tumor) - Untreated coagulopathy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Interlaminar cervical epidural injection
Fluoroscopy-guided interlaminar cervical epidural injection
Cervical selective nerve root block
Ultrasound-guided cervical selective nerve root block

Locations

Country Name City State
Turkey Diskapi Yildirim Beyazit Training and Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Diskapi Teaching and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reduction in pain Pain assessment will be performed using the Numerical Rating Scale (NRS) score (0 = no pain, 10 = the most severe pain felt). Change from baseline pain score to 6months
Secondary Neck Disability Index baseline to 6 months post-procedure
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