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Reliability of MRI and Ultrasound in Cervical Epidural Needle Depth Estimation

Reliability of MRI and Ultrasound in Predicting Needle Depth During Cervical Epidural Injections: a Methodological Observational Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06747663
Acronym
CERV-MRI-USG
Enrollment
90
Registered
2024-12-24
Start date
2025-01-31
Completion date
2025-07-31
Last updated
2024-12-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Epidural Injection, Chronic Neck Pain, Radicular Pain

Keywords

Cervical Epidural Steroid Injection, Needle Depth Estimation, Ultrasound Guidance, MRI Guidance, Fluoroscopy, Radiation Exposure, Chronic Pain Management

Brief summary

This study aims to evaluate the reliability of magnetic resonance imaging (MRI) and ultrasound (USG) in predicting needle depth during cervical epidural injections, compared to fluoroscopy. The goal is to identify alternative imaging methods that reduce radiation exposure while maintaining procedural accuracy and patient safety.

Detailed description

Cervical epidural steroid injections (CESI) are commonly used to manage chronic neck and radicular pain. Accurate needle placement is critical for the success and safety of the procedure. Fluoroscopy is the standard method for guiding the needle; however, it exposes patients and clinicians to ionizing radiation. This study compares pre-procedural MRI and USG measurements of needle depth with fluoroscopy-guided needle depth during CESI. Primary Objective: Assess the agreement between MRI, USG, and fluoroscopy measurements of needle depth using intraclass correlation coefficients (ICC) within a ±0.3 cm tolerance. Secondary Objectives: Evaluate the correlation between fluoroscopic lateral imaging frequency and radiation exposure. The study is a methodological observational study conducted at Ankara Etlik City Hospital, involving adult patients undergoing CESI. Data will be collected retrospectively and prospectively for eligible participants.

Interventions

PROCEDURENeedle Depth Measurement Using MRI, Ultrasound, and Fluoroscopy

This intervention involves cervical epidural steroid injection (CESI) for patients with chronic neck and radicular pain. Needle depth is measured pre-procedurally using MRI and ultrasound to predict the ideal needle placement. Fluoroscopy is used during the procedure to confirm and compare these measurements, aiming to evaluate the accuracy of imaging techniques and minimize radiation exposure.

Sponsors

Ankara Etlik City Hospital
CollaboratorOTHER_GOV
Damla Yürük
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Age ≥ 18 years, Diagnosed with chronic cervical pain, Referred for cervical epidural steroid injection, Patients capable of providing informed consent.

Exclusion criteria

Age \< 18 years, Pregnancy or breastfeeding, History of coagulation disorders or use of anticoagulants, Severe systemic infections or local infections at the injection site, Known allergy to steroids or local anesthetics, Uncontrolled diabetes mellitus, Patients with spinal tumors or significant spinal deformities, Previous cervical spine surgery, Cognitive impairment preventing informed consent or follow-up participation.

Design outcomes

Primary

MeasureTime frameDescription
Accuracy of Needle Depth Prediction Using MRI and Ultrasound Compared to Fluoroscopy in Cervical Epidural Steroid Injections1 day (during the procedure)The primary outcome measure evaluates the reliability and accuracy of pre-procedural needle depth measurements obtained using MRI and ultrasound imaging compared to intra-procedural fluoroscopy during cervical epidural steroid injections. The goal is to determine the concordance between these imaging techniques and assess their utility in reducing procedural radiation exposure.

Secondary

MeasureTime frameDescription
Radiation Exposure During Cervical Epidural Steroid Injections1 day (during the procedure)The secondary outcome measure assesses the level of radiation exposure (in mGy) experienced by patients and practitioners during cervical epidural steroid injections when fluoroscopy is used. Comparisons will be made to determine if the use of pre-procedural MRI or ultrasound reduces fluoroscopy duration and radiation exposure.

Countries

Turkey (Türkiye)

Contacts

Primary ContactDAMLA YÜRÜK, Associate Professor of Algolog
damlayuruk@hotmail.com+905319932378
Backup ContactTAYLAN AKKAYA, Professor of Algolog
damlayuruk@hotmail.com095319932378

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026