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Selective Nerve Root Block for Lumbar Radiculopathy
Phase 4
Waitlist Available
Led By Michael Steinmetz, MD
Research Sponsored by The Cleveland Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12-months
Awards & highlights
Study Summary
Threshold Response of Lumbar Selective Nerve Root Block in Predicting Good Outcome Following Lumbar Foraminotomy
Eligible Conditions
- Lumbar Radiculopathy
- Degenerative Spinal Stenosis
- Back Pain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12-months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12-months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Visual Analog Scale (VAS) Leg Pain Score
Secondary outcome measures
EQ-5D Questionnaire
Oswestry Disability Index Questionnaire (ODI)
Pain Disability Questionnaire (PDQ)
Trial Design
1Treatment groups
Experimental Treatment
Group I: Selective Nerve Root BlockExperimental Treatment1 Intervention
Patient will receive a Selective Nerve Root Block injection at the target level prior to surgical intervention.
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Who is running the clinical trial?
Lumbar Spine Research SocietyUNKNOWN
The Cleveland ClinicLead Sponsor
1,026 Previous Clinical Trials
1,366,065 Total Patients Enrolled
Michael Steinmetz, MDPrincipal Investigator - The Cleveland Clinic
Cleveland Clinic Hospital
Texas Tech University Hlth Sci Ctr School Of Medicine (Medical School)
Cleveland Clinic Fndn (Residency)
1 Previous Clinical Trials
40 Total Patients Enrolled
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