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Fractures, Bone clinical trials

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NCT ID: NCT01051869 Completed - Humeral Fractures Clinical Trials

Simple Decompression Versus Anterior Transposition of the Ulnar Nerve

Start date: September 2010
Phase: N/A
Study type: Interventional

Both simple decompression and anterior transposition of the elbow nerve (ulnar nerve) for acute displaced fractures of the elbow (distal humerus) treated with plate fixation are currently used by surgeons. We want to examine which treatment will overall give better results in regards to arm function and residual pain.

NCT ID: NCT01049191 Completed - Osteoporosis Clinical Trials

Bone Microarchitecture in Women With and Without Fracture

mMRI
Start date: October 2008
Phase: N/A
Study type: Observational

Osteoporosis is a common disorder of compromised bone strength causing 40-50% of women and ~25% of men to sustain fragility fractures during their lifetime. The reduction of bone strength in osteoporotic people results from loss of bone density and deterioration of bone quality. Bone quality is a complex amalgamation including macro- and micro-architecture, mineralization, turnover and damage accumulation. Currently, medications to reduce fracture risk are prescribed primarily on the basis of bone mineral density (BMD) measurement. Unfortunately, currently available BMD measurement technologies do not detect the aforementioned properties of bone quality; as such, less than half of individuals who sustain osteoporotic fractures are classified as "osteoporotic" by currently available diagnostic tools. Clearly, measures to enhance identification of those at high fracture risk are needed. High-resolution magnetic resonance imaging (HR-MRI) technology, such as that provided by MicroMRI, Inc., has outstanding potential to be such a tool. Therefore, our long-term goal is to evaluate and optimize the use of HR-MRI in fracture risk prediction; this pilot work is an essential step in attaining this goal. This research will investigate 72 postmenopausal women with normal or osteopenic BMD by dual-energy x-ray absorptiometry (DXA), 36 with prior low-trauma fractures will be compared with 36 age-, race- and BMD matched women without fracture. We hypothesize that 1.) Women with fractures will have evidence of microarchitectural deterioration on HR-MRI and 2.) Newly developed, more rapid MRI sequences designed at the UW will provide similar trabecular microstructure information more rapidly than the currently used, albeit investigational, technology produced by MicroMRI, Inc. Our specific aims are to a) Evaluate differences in MicroMRI parameters of trabecular microstructure (bone volume fraction, trabecular thickness, surface/curve ratio and erosion index) between age-, race- and BMD-matched postmenopausal women with and without fracture; b.) Correlate T2* relaxation time (a rapid indirect MRI measure of trabecular density and microstructure) with BMD measured by DXA, and microstructural parameters measured by MicroMRI. As an exploratory aim we will investigate HR-MRI parameters of trabecular microstructure obtained using a newly developed, rapid MRI sequence referred to as IDEAL-FSE with parameters obtained using the currently available MicroMRI, Inc. sequence.

NCT ID: NCT01047826 Recruiting - Tibia Fracture Clinical Trials

M.I.P.O. vs Intramedullary Nailing in Tibia Fractures

MINT
Start date: December 2010
Phase: N/A
Study type: Interventional

The investigators are comparing two methods of standard treatments in distal tibial fractures. locked plating (M.I.P.O. technique) with intramedullary nailing. the investigators are hypothesizing that M.I.P.O group is superior to nailing in fractures of the distal third of the tibia.

NCT ID: NCT01035359 Completed - Clinical trials for Dorsally Displaced Intraarticular Distal Radius Fractures

Intraarticular Distal Radius Fractures, X-fix or Volar Fixation

Start date: August 2009
Phase: N/A
Study type: Interventional

Distal radius fractures are treated surgically if severely displaced. This study aims to investigate the outcome after surgery. The investigators will randomize patients to either external fixation with optional addition of k-wires or open reduction and fixation with a volar plate.

NCT ID: NCT01035177 Terminated - Osteoporosis Clinical Trials

In Vivo Hip Fracture Discrimination With Quantitative Computed Tomography (QCT)

FEMFRACT
Start date: February 2005
Phase: N/A
Study type: Observational

Numerous geometric and bone mineral density (BMD) parameters can be derived from quantitative computed tomography (QCT) images of the proximal femur analyzed using dedicated software. The primary objective is to evaluate the contribution of QCT-image analysis to the prediction of the osteoporotic hip fracture risk, as compared to the reference standard, namely, dual energy X-ray absorptiometry (DXA). Study hypothesis: For predicting osteoporotic hip fracture, findings from QCT images of the proximal femur analyzed using dedicated software are superior over DXA measurements of proximal femoral BMD.

NCT ID: NCT01034943 Completed - Clinical trials for Dorsally Displaced Intraarticular Distal Radius Fractures

Extraarticular Distal Radius Fractures, X-fix or Volar Fixation

Start date: August 2009
Phase: N/A
Study type: Interventional

Distal radius fractures are treated surgically if severely displaced. This study aims to investigate the outcome after surgery. The investigators will randomize patients to either external fixation with optional addition of k-wires or open reduction and fixation with a volar plate.

NCT ID: NCT01032356 Not yet recruiting - Clinical trials for Distal Radius Fracture

Dynasplint for Distal Radius Fracture

Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to examine the efficacy of dynamic splinting as a therapeutic modality in reducing contracture following surgical treatment of distal radius fractures.

NCT ID: NCT01017341 Active, not recruiting - Hip Fracture Clinical Trials

Hip Protector for Prevention of Hip Fracture

Start date: June 2010
Phase: Phase 3
Study type: Interventional

This study aims to evaluate the efficacy of the investigators PSU hip protector for prevention of fracture in elderly.The eligible patients include those with previous diagnosed as unilateral hip fracture. They will be randomized into 2 groups;psu hip protector and no protector. The patients will be instructed to wear the protector fulltime.The inceidence of hip fracture will be compared between both group at the end of 1 year.

NCT ID: NCT01017289 Not yet recruiting - Humeral Fractures Clinical Trials

Intramedullary Fixation of Humerus Fractures

Start date: December 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the safety and efficacy of the composite Nail - the Quantum interlocking intramedullary nailing system in the reduction of humeral fractures.

NCT ID: NCT01017094 Completed - Tibial Fracture Clinical Trials

Pin Site Infection Prevention for Open Tibial Fracture

Start date: September 2007
Phase: Phase 3
Study type: Interventional

This study aimed to compare the efficacy of pin-tract infection prevention between silversulfadiazine and dry dressing. Methods: 30 patients with an open tibial fracture admitted to Songklanagarind hospital from September 2007 to June 2008 and treated by emergency debridement and external fixation were randomized into two groups, one treated with silversulfadiazine for infection prophylaxis (15) and a control group treated with dry dressing only (15). All patients were followed until the external fixator was removed. Pin-site infections were assessed and graded at each follow-up visit by an orthopaedist blinded to the mode of treatment. A culture from the pin site was done if an infection occurred.