Radiofrequency Ablation: Treatment for Posterior Element Pain From Vertebral Compression Fractures
Vertebral Compression Fracture, Facet Joint Pain
About this trial
This is an interventional treatment trial for Vertebral Compression Fracture
Eligibility Criteria
I• Inclusion
- 18-90 years old
- Male or female
- Age of fracture greater than or equal to 6 weeks
- Single Level Vertebral Compression Fracture
- Vertebral compression fracture Thoraic-9 to Lumbar-5
NRS >6/10
• Exclusion
- <18 or >90 yo
- Uncorrectable Coagulopathy
- Multiple Level Vertebral Compression Fractures
- Surgery within 60 days of presentation
- Active infection
- Rhuematologic disease
- Significant neurologic deficit
- Radicular pain
- Chronic low back pain in last year
- Inability to give consent
- Cognitive impairment
- Patients with Ongoing Litigation or Worker's Compensation Cases
Sites / Locations
- UC Davis Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Control Group
Treatment Group
Crossover Group
The control group will receive usual care for treatment of vertebral compression fractures, which will consist of but not limited to: physical therapy, opioids, NSAIDs, acetaminophen and bisphosphonates as indicated. They will have the option of crossing over (see "Crossover Group") at twelve weeks.
The treatment group will receive usual care for treatment and the treatment procedure comprised of the Medial Branch Block and Radiofrequency Ablation. In cases where a medial branch nerve block has confirmed there is pain relief, a radiofrequency ablation is considered. These patients will continue their usual care therapy as well.
This group will comprise of patients within the control group who after 12 weeks of usual therapy will have the option of crossing over to the treatment group. Once crossed over, their treatment and course and measurements will be identical to that of the treatment group.