🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in India / NCT07027306
Recruiting

The Osteoporotic Fracture Classification-based Scoring System for Treatment Decision in Thoracolumbar Osteoporotic Fractures

NCT07027306 · tracked via the Priya Life Science India tracker
Sponsor
AO Foundation, AO Spine
Phase
Started
2026-03-19
Last updated
2026-05-13

Condition(s) studied

Osteoporotic FracturesOsteoporosis

Investigational drug(s) / intervention(s)

Posterior stabilization (pedicle screws)

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

Sex
ALL
Min age
50 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Postmenopausal women ≥ 50 years old or men \> 60 years old o Menopause refers to amenorrhea for 1 complete year. * Radiologically confirmed new diagnosis of symptomatic, single or multilevel TL (from T1 to L5) fractures, ie, the index fracture(s). * In case of a multilevel fracture, the fracture must be contiguous. * The index fracture is confirmed by MRI as an insufficiency (or fragility) fracture or is confirmed by CT or MRI as traumatic fracture (low-energy trauma) * The index fracture(s) is a result of primary osteoporosis. Diagnosis of primary osteoporosis is based on any of the followings in the absence of causes for secondary osteoporosis (such as long-term use of steroids, rheumatoid arthritis, type 1 diabetes mellitus \[DM\], and other metabolic bone disorders \[eg, rickets/osteomalacia, Paget's disease, osteogenesis imperfecta, and primary hyperparathyroidism\]) \[13-15\]: * A T-score ≤ -2.5 in the lumbar spine, femoral neck, total hip, or 1/3 radius * Presence of fragility fracture (either a previous fragility fracture or the index fracture is a fragility fracture). Fragility fractures are fractures due to no or low-energy trauma, eg, slips, trips, or falls from less than double the body height, and heavy lifting. * The index osteoporotic TL fracture being classified based on the OF Classification from OF 1 to OF 5: * OF 1: No deformation (vertebral body edema on MRI using short tau inversion recovery \[STIR\] sequence) * OF 2: Deformation of one endplate * OF 3: Deformation of one endplate with distinct posterior wall involvement * OF 4: Deformation of both endplates with/without posterior wall involvement * OF 5: Injuries with anterior or posterior tension band failure * Ability to provide informed consent according to the EC/IRB defined and approved procedures Exclusion Criteria: * Patients with spinal tumors * Patients with concomitant cervical fractures * Patients showing any signs of spinal infections * Patients with fractures due to high-energy or high-impact trauma, eg, a fall from double the body height or higher, motor vehicle accident with \> 100 km/h in cars with airbags, or motor vehicle accident \> 50 km/h without airbags, polytrauma * Patients with concomitant fracture in the pelvis, upper extremities, and/or lower extremities which could affect the main study outcomes (specifically, patient mobility and pain) * Patients for whom no FUs are possible * Previous instrumented surgery in the affected spine levels * Patients with single-level fracture or contiguous multilevel fracture adjacent to previous instrumented surgery * Patients who are mentally impaired and therefore not able to adhere to the study procedures and data collection * Patients who are bedridden before the index fracture * Recent history of substance abuse (ie, recreational drugs and alcohol) that would preclude reliable assessments * Participation in any other medical device or medicinal product study within the previous month that could influence the results of the present study

Primary outcome measure(s)

Trial sites (15)

FacilityCityRegionStatus
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
Official registry record

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