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Femoral Fractures clinical trials

View clinical trials related to Femoral Fractures.

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NCT ID: NCT00626470 Completed - Femoral Fractures Clinical Trials

Prospective Trial on Trochanteric Femur Fractures Treated With or Without a Trochanter Support Plate

TSP
Start date: December 2008
Phase: N/A
Study type: Interventional

Fractures just below the hip often are treated with a so called Gliding Screw and Plate (DHS). Recently a new additional plate called a Trochanter Support Plate (TSP) which attaches to the DHS has become available which is claimed to give extra support to the fracture. In a prospective randomised study we wish to test the hypothesis that the TSP does not give any additional stability to the fracture treated with the DHS.

NCT ID: NCT00621088 Completed - Clinical trials for Trochanteric and Subtrochanteric Hip Fractures

A Prospective Randomised Multicenter Study Comparing the Sliding Hip Screw and the Intertan Nail in Trochanteric and Subtrochanteric Femoral Fractures

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

This is a study to compare the new nail "INTERTAN" with a Sliding Hip Screw in treating a specific group of hipfractures (trochanteric and subtrochanteric fractures). Are there differences in terms of pain, early and late functional mobility and complications between the to implants (and methods of operation)?

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.

NCT ID: NCT00593333 Completed - Femur Fracture Clinical Trials

Intramedullary Nailing of the Femur:Trochanteric vs Piriformis Starting Portals

TROCHNAIL
Start date: June 2003
Phase: N/A
Study type: Interventional

This project is designed to determine whether or not the trochanteric insertion portal will show any difference when compared with the piriformis fossa portal in terms of pain and strength of the hip abductor muscles, while allowing faster surgical fixation of the femur fracture.

NCT ID: NCT00578019 Completed - Clinical trials for Supracondylar Femur Fracture

Comparison Between LISS Plating and Intramedullary (IM) Nailing for Supracondylar Femur Fractures

LISS
Start date: December 1999
Phase: N/A
Study type: Interventional

The purpose of this study is to compare patient outcomes for the Less Invasive Stabilization System (LISS) (Synthes {USA}, Paoli, PA, USA), a minimally invasive plating system used in the treatment of supracondylar femur fractures, with patient outcomes for the Supracondylar Nail (Smith & Nephew Inc, Memphis, TN, USA), a retrograde intramedullary nail.

NCT ID: NCT00552331 Completed - Femoral Fractures Clinical Trials

Evaluation of the Effects of Less Invasive Stabilization System (LISS) Plating Techniques in Distal Femoral Fractures

Start date: March 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the rate of fracture healing and fracture union, repaired with the LISS device, will be as good as or better than the usual fracture fixation systems.

NCT ID: NCT00546429 Completed - Clinical trials for Femoral Fracture (Proximal)

DePuy Trochanteric (ATN) Nailing Clinical Outcomes Trial

ATN
Start date: September 1, 2006
Phase:
Study type: Observational

The purpose of this study is to monitor trochanteric fracture healing and review the performance of the ATN system.

NCT ID: NCT00534326 Completed - Femoral Fractures Clinical Trials

Standard Reaming Versus Reaming/Irrigating/Aspirating for Intramedullary Nailing of Femoral Shaft Fractures

STAFF
Start date: December 2006
Phase: N/A
Study type: Interventional

Reaming (enlarging of the bone canal) is commonly performed prior to the insertion of intramedullary nails for the fixation of long bone fractures. This study is designed to compare the union rates between fractures reamed by standard reaming versus reaming with a Reamer/Irrigator/ Aspirator (RIA). In addition, this study will collect patient-based outcomes on these patients. Little information exists on the patient based outcomes following femur fractures. We hope that the patient based outcomes of this study will also be able to aid physicians in advising patients with femur fractures of their possible outcomes.

NCT ID: NCT00521716 Suspended - Hip Fracture Clinical Trials

Safety and Efficacy of the WaisFix100i for Intracapsular Femoral Fracture Fixation

Start date: September 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of using WaisFix100i device for Intracapsular Femoral Fracture Fixation.