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Fractures, Bone clinical trials

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NCT ID: NCT01214291 Withdrawn - Clinical trials for Risk of Bone Fracture Occurrences

Efficacy and Safety Study of Toremifene Citrate for the Reduction in the Risk of New Bone Fracture Occurrences in Men With Prostate Cancer

TREAT2
Start date: March 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether Toremifene Citrate is effective in reducing the risk of bone fractures in men with prostate cancer who are on Androgen Deprivation Therapy.

NCT ID: NCT01206179 Completed - Nonunion Fractures Clinical Trials

Treatment of Non Union of Long Bone Fractures by Autologous Mesenchymal Stem Cell

Start date: March 2009
Phase: Phase 1
Study type: Interventional

Treatment of nonunion, delayed union and malunion fractures of long bones remains problematic. The definition of nonunion is a failure of the fracture to heal in six months in a patient in whom progressive repair had not been observed radiographically between the third and sixth month after the fracture. First of all good surgical techniques are stable immobilization must be obtained and local sepsis excluded. Then stimulation of the callus is required. Numerous techniques have been developed ranging from invasive interventions (including internal fixation with the use of bone graft or bone graft substitutes) to non invasive procedures (ultrasound and pulsed electromagnetic fields). Recently, autologous cell therapy was presented as an interesting approach. The concept of such therapies is based on the effect of stem cells presented in the bone marrow and able to be transformed in osteoblast cells. The purpose of this study is to find if mesenchymal stem cells can stimulate bone regeneration in nonunion and delayed union fractures to reduce later surgeries required to augment the healing process and to accelerate the time to healing.

NCT ID: NCT01200277 Completed - Osteoporosis Clinical Trials

A Trial of Vertebroplasty for Painful Acute Osteoporotic Vertebral Fractures

VertosIV
Start date: January 2011
Phase: Phase 3
Study type: Interventional

The standard care in patients with a painful osteoporotic vertebral compression fracture (VCF) is conservative therapy. Percutaneous vertebroplasty (PV), is a new minimally invasive technique for pain treatment in which bone cement is injected in the fractured vertebra. Recent RCTs provide conflicting results: two sham-controlled studies show no benefit of PV while an unmasked but controlled RCT found significantly better pain relief after PV at acceptable costs.

NCT ID: NCT01199653 Completed - Fracture Clinical Trials

Study Comparing Plate Stabilization to Conservative Treatment in Midshaft Clavicle Fractures

Start date: August 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to find whether to operate or treat conservatively dislocated midshaft clavicle fractures.

NCT ID: NCT01190709 Completed - Clinical trials for Tibial Shaft Fracture

Study of Tibial Shaft Fracture Fixation: Intramedullary Nailing Comparing With Dynamic Compression Plate

Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine which surgical approach is better for treatment of tibial shaft fracture

NCT ID: NCT01190696 Completed - Clinical trials for Femoral Shaft Fracture

Titanium Elastic Nailing Versus Hip Spica Cast in Treatment of Femoral Fractures in Children

Start date: February 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine which method is better for treatment of femoral fracture in children in outcomes.

NCT ID: NCT01183078 Completed - Tibial Fractures Clinical Trials

Distal Locking Using an Electromagnetic Field Guided Computer Based Real Time System for Orthopaedic Trauma Patients

Sure Shot
Start date: August 2010
Phase: N/A
Study type: Interventional

Hypothesis: Utilization of the "wand" method will enhance improvements in drill placement, locking nail placement during tibia and femur fracture repairs, and offer less radiation exposure and less operative time. The purpose of this research study is to compare the efficacy of distal locking of intramedullary nails using a standard free-hand technique with the guided wand technique. Distal locking is the placement of screws through the intramedullary rod to hold it in place and prevent rotation. Currently, the free-hand technique is most often utilized. With this technique, the surgeon uses intraoperative x-rays in order to find the holes in the intramedullary rod to place the screws. The wand technique uses electromagnetic fields rather than x-rays to find these screw holes. The utilization of the wand technique could result in improvements in drill placement and locking nail placement as well as decrease operative time and radiation exposure.

NCT ID: NCT01181037 Recruiting - Clinical trials for Displaced Subcapital Femoral Fracture

Bipolar H.A Versus Trochanteric Antegrade Nail for Treatment of Displaced Subcapital Femoral Fractures

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

A retrospective study to compare clinical results of patients that were treated by Bipolar H.A. vs. closed reduction and internal fixation with Trochanteric Antegrade Nail for displaced femoral subcapital fracture.

NCT ID: NCT01174589 Completed - Hip Fracture Clinical Trials

Training of Patients With Hip Fracture

Start date: September 2010
Phase: Phase 2
Study type: Interventional

The primary purpose of this study is to illustrate whether there is a difference in the 6 minutes walking test in patients with hip fractures who have received 6 vs. 12 weeks of physical training after discharge from hospital.

NCT ID: NCT01173744 Recruiting - Clinical trials for Intertrochanteric Femoral Fractures

Comparison of Gamma Nail Versus Dynamic Hip Screw for the Treatment of Unstable Intertrochanteric Fractures

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

The objective of the study is to examine the treatment of unstable Intertrochanteric fractures with the short Gamma nail, compared to the use of the dynamic hip screw (DHS). This is a prospective study. Sixty patients with unstable Intertrochanteric fractures will be randomized to be treated using either Gamma nail or DHS. The patients will be followed for 12 months. The primary endpoint is the clinical outcome as measured by the Merle d'Aubigne and Postelhip score.