Vertebral Compression Fracture Clinical Trial
Official title:
VertebrOpLasty Versus Conservative Treatment in Acute Non Osteoporotic Vertebral Fractures
The purpose of this protocol is to prove the efficacy of vertebroplasty in patients
suffering from acute non osteoporotic vertebral compression fracture.
Vertebroplasty consists in the injection of cement (PMMA) in the damaged vertebral body to
prevent further collapse.
Our study will compare vertebroplasty versus conservative therapy (brace).
The study is a prospective, randomized trial comparing conservative treatment (brace) and vertebroplasty in acute (less than 15 days after trauma) traumatic vertebral compression fracture (VCF) type A according Magerl classification ;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Enrolling by invitation |
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|
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| Completed |
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|
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| Completed |
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|
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| Suspended |
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Radiofrequency Ablation: Treatment for Posterior Element Pain From Vertebral Compression Fractures
|
Phase 4 |