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Fractures, Bone clinical trials

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NCT ID: NCT01505985 Terminated - Hip Fracture Clinical Trials

Hip Fracture Surgery and Oral Nutritional Supplements

HIATUS
Start date: January 2012
Phase: Phase 3
Study type: Interventional

Senior hip fracture patients are the most vulnerable to malnutrition and protein deficiency. Low protein intake, like vitamin D deficiency, contribute to an increased risk for hip fracture. Notably, several clinical trials with protein supplementation in senior hip fracture patients resulted in fewer deaths, shorter hospital stay, and a higher likelihood of return to independent living. The proposal is to test the effect of an oral nutritional supplement (ONS) which has been designed to meet the specific nutrient needs of senior bone and muscle health. The hypothesis is that this ONS will improve functional recovery after hip fracture (as measured by Short Physical Performance Battery (SPPB)), improve quality of life, improve muscle mass, and- decrease falls and hospital re-admission after hip fracture.

NCT ID: NCT01504568 Withdrawn - Orbital Fractures Clinical Trials

The Use of Prophylactic Antibiotics in Isolated Blowout Fractures

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of the research is to perform a quality assurance evaluation using randomized prospective analysis the rate of orbital cellulitis as a complication of nonsurgical orbital blowout fracture in patients treated versus not treated with prophylactic antibiotics. The investigators goal is to show the use of prophylactic antibiotics in orbital blowout fractures does not significantly decrease the rate of orbital cellulitis and is thus not indicated.

NCT ID: NCT01497080 Completed - Clinical trials for Radius Fracture Distal

Distal Radius Fracture Prospective Database 50-80 Years Old

Start date: January 2012
Phase: N/A
Study type: Observational

The Problem Distal radius fractures (DRF) are common and result in a variable amount of disability. The investigators have completed considerable work in developing tools that measure impairment and disability after DRF . The investigators initial studies indicate that the associated disablement process is multifactorial and variable with only 25% of the resultant disability predicted by baseline patient and injury characteristics. The investigators see DRF as a signal event where some people are at-risk of transitioning from an active lifestyle to inactivity and subsequent health risks. The investigators recent data confirms variable participation following a DRF. The traditional focus in orthopedic/rehabilitative approaches to DRF fracture management has been localized to the wrist, largely ignoring this potential transition and its health impacts. The investigators will initiate a line of investigation that will profile the at-risk older adult who presents with a DRF with the ultimate goal of accurate identification and prevention of adverse activity transitions (active to inactive). In this study the investigators will identify the extent of the problem by quantifying changes in activity/participation and its short-term health impacts. The investigators will also identify the risk factors present at time of injury that predict a loss of mobility/activity/participation. This work has the potential to identify tools and/or clinical prediction rules that identify at-risk individuals at a critical time where early intervention might most easily prevent adverse outcomes associated with inactivity.

NCT ID: NCT01494519 Completed - Clinical trials for Severe Open Fractures of the Tibia (Shin) Bone

Assessment of Fixation Strategies for Severe Open Tibia Fractures

FIXIT
Start date: July 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the use of modern ring external fixation versus internal fixation for fracture stabilization of severe open tibia fractures.

NCT ID: NCT01494090 Terminated - Hip Fracture Clinical Trials

Statin in Hip Fracture

STAFF
Start date: August 2011
Phase: Phase 3
Study type: Interventional

Statins (or HMG-CoA reductase inhibitors) have largely proven their efficacy in the primary and secondary prevention of cardiovascular events. Many clinical and experimental studies support also a potential beneficial effect of statin therapy on venous thromboembolism (VTE). Patients with hip fracture are at high risk of VTE and cardiovascular events. The aim of this study is to evaluate the efficacy and the tolerance of a statin (rosuvastatin) in hip fracture surgery on the occurrence of venous and atherothrombotic events and the global mortality at six months. Subjects aged 60 years or over who are scheduled to undergo surgery for fracture of the upper portion of the femur (hip fracture) are eligible to participate to this multicentre, randomized, double-blind placebo controlled trial. They will receive either rosuvastatin (5 or 20 mg) or placebo for 6 months. The primary efficacy outcome is the incidence of an adjudicated composite of non fatal VTE, acute coronary syndrome, non fatal stroke, other acute ischemic arterial event, or all-cause death. Assuming a endpoint frequency of 20% in the control group, we calculated that 1200 patients will be required for the study to have 80% power to detect a 30% reduction in the relative risk with rosuvastatin (with a two-sided alpha level of 5%). The investigators assumed that rosuvastatin could have a positive benefit-risk ratio in patients undergoing orthopaedic surgery for hip fracture, by reducing vascular events and global mortality at six months.

NCT ID: NCT01493167 Completed - Bone Fracture Clinical Trials

Study on Wood-plastic Composite for Circumferential Casting

WOODCAST
Start date: December 2011
Phase: N/A
Study type: Observational

The purpose of study is to verify that WOODCAST Circular system performs safely and effectively in its intended use.

NCT ID: NCT01488812 Completed - Hip-fracture Clinical Trials

Waiting Time to Operation for Hip-fracture Patients

Start date: May 2010
Phase: N/A
Study type: Observational

This study investigates the relationship between waiting time to surgery and the risk for medical complications and 1-year mortality in hip-fracture patients.

NCT ID: NCT01487772 Completed - Hip Fractures Clinical Trials

Improving Quality of Care for Hip-Fracture Patients: Studies on Fast-track Surgery

Q-HIP
Start date: April 2010
Phase: N/A
Study type: Observational

The aims of the studies are to examine the impact of delayed time to surgery for hip-fracture patients with regard to in-hospital complication rate and one-year mortality and to evaluate two different fast-track systems for hip-fracture patients with regard to patient outcome, complication rate and patient satisfaction.

NCT ID: NCT01484535 Completed - Ankle Fracture Clinical Trials

Aspiration for Pain Relief Following Ankle Fracture

Start date: September 2011
Phase: N/A
Study type: Interventional

This trial will study the effect of hematoma aspiration in patients with acute ankle fractures.

NCT ID: NCT01484405 Terminated - Femur Fracture Clinical Trials

Anterolateral Versus Posterior Approach for Total Hip Arthroplasty After Displaced Femoral Neck Fracture

THA
Start date: June 2010
Phase: N/A
Study type: Interventional

There are two surgical approaches (incision types) used by surgeons who do total hip replacements. The purpose of this study is to determine which type of surgical approach (incision type) produces the best results for patients who have a total hip replacement. Null Hypothesis : There is no difference in complication rate, functional outcome, surgical time, or blood loss when comparing outcomes in patients receiving THA to hemiarthroplasty or ORIF for femoral neck fractures.