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Spinal Trauma clinical trials

View clinical trials related to Spinal Trauma.

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NCT ID: NCT05856370 Recruiting - Spinal Deformity Clinical Trials

The Ailliance Post-Market Clinical Study

Start date: May 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s). Subjects are enrolled and followed postoperatively for up to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.

NCT ID: NCT01643395 Completed - Clinical trials for Vertebral Compression Fracture

VertebrOpLasty Versus Conservative Treatment in Acute Non Osteoporotic Vertebral Fractures

VOLCANO
Start date: September 2010
Phase: Phase 3
Study type: Interventional

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).

NCT ID: NCT01433536 Terminated - Healthy Clinical Trials

Evaluation of Circulating Osteogenic Factors in Trauma Patients

BMP-9
Start date: December 2010
Phase: N/A
Study type: Observational

Bone fractures in traumatic brain-injured and spinal cord-injured patients often heal faster than in other patients. However, such patients are also occasionally prone to bone formation in soft tissues such as muscle. This process is called heterotopic ossification and tends to occur around joints. Patients with heterotopic ossification often suffer from complications such nerve compression, ankylosis, chronic pain, osteoporosis, and infections. Loss of movement can also interfere with function and the quality of life of patients already experiencing difficulties associated with their trauma. Positioning, transfers, and hygiene become difficult and even impossible, which worsens the loss of autonomy. Previous research has suggested that an osteoinductive factor (which has the capacity to induce the formation of bone) may be released into the bloodstream following a head or spinal cord injury. The investigators laboratory has shown that a growth factor called BMP-9, when injected into a damaged mouse muscle, has the ability to cause strong ossification in damaged muscle. The investigators would like to find out whether the levels of BMP-9 and/or its receptor (which is called ALK1) increase after traumatic brain and spinal cord injuries that occur at the same time as serious orthopaedic traumas. The main goal of the investigators study is thus to determine whether BMP-9 levels increase in the serum of trauma patients.

NCT ID: NCT01372592 Completed - Spinal Deformity Clinical Trials

SpineTRACK Registry - Spinal Outcomes Registry

Start date: March 2011
Phase:
Study type: Observational

The Spine TRACK Spinal Surgery Registry is a prospective multi-center observational data collection initiative, to capture clinical and radiographic outcomes in candidates for spine surgery with degenerative, deformity, and traumatic pathologies. As an observational database, there are no initial driving hypotheses, but rather data will be mined to answer unforeseen questions, but which may include broad topics such as comparative effectiveness between and among various surgical treatment options, and/or outcomes in various subgroups of patients such as defined by demographics, comorbidities, indications and symptoms, treatment variables, and/or outcome variables.