Clinical Trials Logo

Femur Fracture clinical trials

View clinical trials related to Femur Fracture.

Filter by:

NCT ID: NCT01293916 Completed - Femur Fracture Clinical Trials

Spica Casting in Pediatric Femur Fractures: Study of Single Leg Versus Double Leg Spica Casts

Start date: June 2006
Phase: N/A
Study type: Interventional

Prospective randomized controlled trial comparing use of single leg spica with double leg spica casts in the treatment of pediatric femur fractures in children ages 2 through 6 years old.

NCT ID: NCT00943332 Completed - Femur Fracture Clinical Trials

Pediatric Femur Research Project

Start date: June 2009
Phase:
Study type: Observational

Current treatment protocol for pediatric femoral shaft fractures is immediate spica casting for patients 6 years and younger and for patients over 6 years and older is percutaneous or open placement of titanium elastic intramedullary nails. The investigators would like to evaluate the current treatment protocol by comparing those patients 6 years and younger treated with closed reduction and spica casting to those 6 years and younger treated with percutaneous pinned with titanium elastic intramedullary nails or submuscular plating. The investigators will be comparing their post-operative functional level, pain management, impact on family and complications through chart and x-ray reviews. The goal is to improve patient care pre and post-operatively for those who have sustained a femoral shaft fracture 6 years old and younger and increase the knowledge of those residents/physicians who care for this patient population.

NCT ID: NCT00919464 Terminated - Femur Fracture Clinical Trials

Natural History of Anterior Compartment Pressures of the Thigh Following Femur Fracture

Start date: April 2006
Phase: N/A
Study type: Interventional

This study is to determine the natural history of compartment pressures in the anterior thigh secondary to a fracture of the femoral shaft.

NCT ID: NCT00916136 Completed - Femur Fracture Clinical Trials

Skeletal Versus Cutaneous Traction For Treatment of Femur Fractures

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

The purpose of this study is to determine whether there are any differences in skeletal or cutaneous traction for the treatment of femur fractures.

NCT ID: NCT00888160 Completed - Femur Fracture Clinical Trials

Timing of Orthopaedic Surgery in the Multiply-injured Patient: Development of a Protocol for Early Appropriate Care

Start date: September 2010
Phase:
Study type: Observational

Early fixation of unstable fractures of the femur, pelvis, and acetabulum reduces some complication rates. However, in patients with multiple injuries, the optimal treatment of skeletal trauma may be affected by severe injury to the head, chest, or abdomen. The relationship between associated injury severity and the timing of definitive management of unstable fractures is not well-understood. The practice of "early total care," early definitive fracture management, has been criticized by some, who have suggested that additional hemorrhage with surgery may be associated with a deleterious systemic inflammatory response. The alternative extreme of "damage control orthopedics (DCO)" has been recently proposed as a means of providing provisional stability of major skeletal injury, generally through external fixation. It is speculated that DCO will diminish the potential for systemic compromise. However, the need for further (definitive) surgery on a delayed basis, and the potential additional complications and costs associated with this strategy are controversial. The investigators' goals are to define which injuries or parameters warrant delay of definitive orthopaedic care, and to determine what time interval for fracture fixation promotes optimal patient outcome. The investigators will assess the effects of fracture fixation on head injury, chest injury, abdominal injury, mortality, complications, patient outcomes, and costs.

NCT ID: NCT00793637 Completed - Femur Fracture Clinical Trials

Evaluation of Handling and Possible Complications Related to the Newly Developed Angular Stable Locking System (ASLS)

ASLS-Pre
Start date: August 2008
Phase:
Study type: Observational

In many cases, the existing locking bolts and screws in intramedullary nails do not provide sufficient stability. Due to the play between screw and nail, the reduction can be lost and the instability can result in malunions, nonunions, or pseudoarthrosis. Consequently, secondary angular fracture dislocation (defined as a difference of the angle of 10° or more from the post-operative to the follow-up x-rays) can be observed in approximately 30% of patients after conventional intramedullary nailing of proximal third tibial fractures and in approximately 0-2% in patients with distal third tibial fractures. Therefore, an Angular Stable Locking System for Intramedullary Nails (ASLS) was developed to reduce the risk of secondary loss of reduction by providing axial and angular stability. ASLS provides angular stable fixation between nails and screws with resorbable sleeves used as dowels in the nail locking holes. The present study evaluates the handling of ASLS and the surgeon's compliance as well as any complications occurring during the baseline and the follow-up period in patients with proximal and distal tibial, femoral and humeral fractures treated with intramedullary nails. Furthermore, the relationship of any occurred complications to ASLS will be assessed.

NCT ID: NCT00725894 Completed - Femur Fracture Clinical Trials

Pediatric Locking Nail for the Treatment of Femoral Fractures in Children

PLN
Start date: November 2007
Phase: N/A
Study type: Observational

The purpose of this multi-center prospective clinical outcomes study is to determine validity and safety of the pediatric locking nail for femoral fracture management in children with open physes.

NCT ID: NCT00686023 Not yet recruiting - Femur Fracture Clinical Trials

Comparing Surgical Techniques for CRIF of Pertrochanteric Fractures

Start date: June 2008
Phase: N/A
Study type: Interventional

Hypothesis: Inflatable intra medullary femoral nailing is superior to DHS in terms of blood loss, operative complications and postoperative rehabilitation in the management of pertrochanteric femur neck fractures.

NCT ID: NCT00616044 Not yet recruiting - Hip Fractures Clinical Trials

Continuous Spinal Anesthesia Versus Combined Spinal Epidural Block

Spinocath
Start date: March 2008
Phase: N/A
Study type: Interventional

In major orthopaedic surgery of the lower extremities both continuous spinal anesthesia (CSA) and combined spinal epidural anesthesia (CSE) are safe and reliable anaesthesia methods. Our results suggest that both continuous spinal anesthesia and combined spinal epidural anesthesia provide good surgical conditions with a low incidence of complications. The sensory block level and hemodynamic changes were lesser with CSA.

NCT ID: NCT00594438 Completed - Femur Fracture Clinical Trials

Randomized, Prospective Comparison of Two Femoral Reaming Systems

RIA
Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the quantity of fat that is released into the venous system (blood) by reaming the femoral canal during intramedullary nailing of the femur using two different reaming systems.