KCT0009265
Completed
未知
Exploratory Clinical Trial to Evaluate the Efficacy and Safety of Lumbar Cervical Interforaminal Epidural Nerve Block Using the Navigation Plus System, A Randomized, Single-blind, Single-center, Prospective trial (Investigator-initiated)
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Diseases of the musculoskeletal system and connective tissue
- Sponsor
- Korea University Anam Hospital
- Enrollment
- 28
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Age 20 years or older
- •2\) Neurological symptoms such as low back pain or unilateral lower extremity radicular pain due to adhesions or inflammation in the anterior epidural space of the lumbar spine based on imaging examination (CT or MRI) and physical examination. However, they do not show symptoms of paralysis or sensory loss.
- •3\) Voluntarily agree to participate in the clinical trial and provide written informed consent.
Exclusion Criteria
- •1\) blood coagulation disorder (INR \> 1\.5 or platelet count \< 100,000/cm2 ) or taking anticoagulants
- •2\) Have a systemic or injection site infection
- •3\) Allergic to any medication (contrast, local anesthetic, steroids)
- •4\) Allergic to adhesives (adhesives)
- •5\) Pregnant or lactating women
- •6\) Have difficulty prone position
- •7\) Those who are considered for surgical treatment due to neurological impairment
- •8\) Those who are unable to complete pain assessments or questionnaires for the study due to cognitive decline
- •9\) Participation in other clinical trials within 1 month of the screening date
- •10\) Other conditions that, in the opinion of the investigator, make participation in the study inappropriate.
Outcomes
Primary Outcomes
Not specified
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