The Osteoporotic Fracture Classification-based Scoring System for Treatment Decision in Thoracolumbar Osteoporotic Fractures
Condition(s) studied
Investigational drug(s) / intervention(s)
Posterior stabilization (pedicle screws): * Any other type of solely vertebral augmentation (stents, etc.), specify * Posterior stabilization (pedicle screws) * Posterior stabilization (pedicle screws) with kyphoplasty/vertebroplasty * Posterior stabilization (pedicle screws) with screw augmentation * Posterior stabilization (pedicle screws) with screw augmentation and kyphoplasty/vertebroplasty * Posterior stabilization (pedicle screws) with vertebral osteotomy (pedicle subtraction osteotomy or similar) * Combined posterior and anterior stabilization
Study summary
This is an international multicenter prospective observational study. Patients with radiologically confirmed, symptomatic, single- or multilevel contiguous TL (from T1 to L5) fractures as a result of primary osteoporosis will be recruited from participating clinics/hospitals (ie, study sites). Fractures included are insufficiency fractures (confirmed by magnetic resonance imaging \[MRI\]) and traumatic fractures (low-energy trauma, confirmed by computed tomography \[CT\] or MRI).
Eligibility
Primary outcome measure(s)
- Return to mobility — From day of treatment to the end of the first 3 months after treatment.
Determination in patients with symptomatic osteoporotic TL fractures whether an initial treatment adhering to the OF score recommendations (the Accordance group) generates better short-term patient outcomes regarding time to return to mobility level before injury or symptom onset within 3 months after treatment compared to an initial treatment decision not adhering to the OF score recommendations (the Discordance group). The primary outcome of the study is return to the mobility level. Patients will be instructed to evaluate their overall mobility level in reference to their pre-injury or pre-symptom mobility status. This primary outcome will be reported by the patient and measured on a continuous scale of 0 to 100 (0 = no return at all, 100 = full return). Primary endpoint of the study is the time (days) to return of pre-injury or pre-symptom mobility level within 3 months after Day 0. Threshold of returning is defined as ≥ 80 on the continuous scale.
Trial sites (15)
| Facility | City | Region | Status |
|---|---|---|---|
| University of California San Francisco (USCF) Department of Orthopaedic Surgery | San Francisco | California | Not Yet Recruiting |
| Thomas Jefferson University Hospital | Philadelphia | Pennsylvania | Not Yet Recruiting |
| Sanatorio Güemes | Buenos Aires | Argentina | Not Yet Recruiting |
| Cajuru University Hospital | Curitiba | Brazil | Not Yet Recruiting |
| Department of Orthopedic Surgery, Clinica Alemana de Santiago | Santiago | Chile | Not Yet Recruiting |
| Orthopaedic Department, Assiut University Hospitals, Faculty of Medicine | Asyut | Egypt | Not Yet Recruiting |
| Tampere University Hospital | Tampere | Finland | Not Yet Recruiting |
| Center for Spinal and Scoliosis Surgery, Malteser Waldkrankenhaus St. Marien | Erlangen | Germany | Not Yet Recruiting |
| PGIMER - Postgraduate Institute of Medical Education and Research | Chandigarh | India | Not Yet Recruiting |
| Dokkyo Medical University Hospital | Tochigi | Japan | Not Yet Recruiting |
| Island Hospital Spine Centre | George Town | Malaysia | Recruiting |
| Spiatlul Clinic De Urgenta, "Profesor Doctor Nicolae Oblu" | Iași | Romania | Recruiting |
| Security Force Hospital | Riyāḑ | Saudi Arabia | Recruiting |
| Spital Emmental - Orthopädie Sonnenhof | Burgdorf | Switzerland | Not Yet Recruiting |
| King's College Hospital | London | United Kingdom | Not Yet Recruiting |
More AO Foundation, AO Spine trials in India
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07027306 on ClinicalTrials.gov ↗ ← All trials in India