Comparison of cervical 6-7 approach with cervical 7- thoracic 1 approach for cervical interlaminar epidural injectio

Not Applicable

Recruiting

• Conditions: Diseases of the musculoskeletal system and connective tissue

• Registration Number: KCT0008358
• Lead Sponsor: Asan Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Patients scheduled for cervical epidural block at C6-7, C7-T1 level
- 20 = age <80
- Patients with one or two levels of cervical HIVD or foraminal or central stenosis on MRI
- Patients who voluntarily gave written consent to participate in this clinical trial

Exclusion Criteria

- Patients with side effects from local anesthetics, steroids, or contrast agents
- Those who have contraindications to nerve block such as blood coagulation disorder or infection
- Patients with red signs of infection, malignant tumor, vertebral fracture, progressive neurological deficit, cauda equina syndrome, etc.
- Patients with neurological or psychiatric problems
- pregnancy
- If the patient does not agree to participate in the study
- In case of cervical spine surgery
- Patients whose epidural space is not visible due to severe stenosis at the injection site

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The ratio of reaching the target level of the cervical vertebrae of the contrast medium administered with a certain dose, the range of diffusion above or below the injection point of the contrast medium

Secondary Outcome Measures

Name	Time	Method
umerical Pain Ratings in the Neck or Upper Extremity;neck disability index;medication quantification sacle;global perceived effect;patient health questionnaire-9(PHQ-9)