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Fractures, Bone clinical trials

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NCT ID: NCT01352754 Active, not recruiting - Hip Fracture Clinical Trials

Troponin T Elevation in Patient Undergoing Hip Fracture Surgery

Start date: April 2011
Phase: N/A
Study type: Observational

Background: Patients undergoing hip fracture surgery are elderly and usually have co-morbidities; hence they are at risk for perioperative MI. Troponin is the gold standard for diagnosis of myocardial damage and currently the cornerstone of MI diagnosis. Perioperative troponin elevation is a poor prognosis factor. The significance of minor troponin elevation, detected by highly sensitivity troponin T assay, is unknown. Objectives: To determine the frequency of perioperative troponin T elevation using highly sensitivity troponin T assay, and to determine the clinical significance of this elevation. Methods: Serum Troponin T levels of patients undergoing hip fracture surgery will be tested prior to surgery 48 hrs and 72 hrs after surgery, using highly sensitivity troponin T assay. Patients will be followed for 1 year. Primary outcomes- The number of patients with elevated troponin levels perioperatively and cardiac mortality at 3 months, 6 months and 1 year.

NCT ID: NCT01352039 Terminated - Clinical trials for Hip Fracture Surgery

A Non-inferiority Study Comparing Two Heparin Sodium Preparations in Hip Fracture Surgery

HEP-SC
Start date: October 2011
Phase: Phase 3
Study type: Interventional

The primary objective and endpoints of the study is compare the efficacy of two products containing heparin sodium, evaluating if the formulation produced by Eurofarma can be considered non-inferior to the reference product.

NCT ID: NCT01350557 Completed - Hip Fracture Clinical Trials

Three Care Models for Elderly Patients With Hip Fracture

Start date: January 2005
Phase: N/A
Study type: Interventional

Hip fracture in the elderly is associated with excess mortality of 5 to 20%, and mobility problems that usually results in costly hospital stays and lengthy rehabilitation procedures. The purpose of this study is to compare the costs and effectiveness of three care models- acute/sub-acute, comprehensive, and routine care models for hip fractured elders in Taiwan.

NCT ID: NCT01344785 Completed - Clinical trials for Intertrochanteric Fractures

The Effect of Loss of Offset After Pertrochanteric Fracture Treated With a Intramedullary Nail

PLAIN
Start date: April 2010
Phase: N/A
Study type: Observational

The purpose of this study is determine the relationship between pain and protrusion of the implant after surgery for a intertrochanteric fracture.

NCT ID: NCT01344772 Completed - Clinical trials for Femoral Neck Fracture

Total Hip Arthroplasty Compared to Internal Fixation for Displaced Intracapsular Fractures of the Femoral Neck

Start date: February 1990
Phase: N/A
Study type: Interventional

The primary aim of this study was to determine the Harris hip score as an evaluation of hip function, in mentally competent elderly patients (>65 years old) treated with either THR or IF, after contracting a displaced femoral neck fracture. The secondary aim was to compare the rate of reoperations and complications between the two groups.

NCT ID: NCT01344343 Completed - Hip Fractures Clinical Trials

HIP Fracture Accelerated Surgical TreaTment And Care tracK (HIP ATTACK) Trial

HIPATTACK
Start date: July 2011
Phase: N/A
Study type: Interventional

There is preliminary evidence that suggests early surgical treatment of a hip fracture may improve patients' outcomes. The investigators propose to do a pilot randomized controlled trial (RCT) to assess the feasibility of a large RCT comparing accelerated surgical repair (i.e. surgery within 6 hours of a hip fracture diagnosis) versus standard care (typically surgery after 36-48 hours).

NCT ID: NCT01341418 Completed - Tibial Fractures Clinical Trials

Suprapatellar Versus Infrapatellar Nailing in Tibial Fractures: A Pilot Study

SP-Pilot
Start date: April 2011
Phase: N/A
Study type: Interventional

This study compares two techniques for the fixation of tibial fractures. The techniques are the suprapatellar (above knee)or infrapatellar (below knee) approach to tibial intramedullary nailing. Null hypothesis: There is no difference in 1) residual post-operative pain levels, 2)knee function, 3) healing and alignment of the tibia, or 4) trochlear changes in the patello-femoral cartilage between patients who are randomized to receive tibial nail insertion through either a suprapatellar nail entry portal or a standard patellar tendon approach.

NCT ID: NCT01341015 Completed - Ankle Fracture Clinical Trials

Bedside Ultrasound in the Diagnosis of Ankle Fractures in Children

Start date: June 2010
Phase: Phase 0
Study type: Interventional

Objectives: A lot of children who injure their ankles come to the emergency department for an evaluation, and often an X-ray of the ankle is obtained to determine if a bone fracture is present. In more than 85% of cases, however, the injury is a sprain and not a bone fracture and can be treated with rest, ice, elevation, and pain medications. X-rays obtained in the emergency departments are time consuming, often uncomfortable for the patient, and expose children to radiation, the long-term effects of which are not yet fully understand by doctors or scientists. Bedside ultrasound is a non-invasive and a non-painful device that does not produce radiation. It was been shown to determine the presence of bone fracture in childrens' wrists and forearms just as well as X-rays do. In our study, the investigators would like to determine if a bedside ultrasound can also be used to evaluate ankle fractures in children. Research Procedures: In our study, the investigators will ask the parents and children, who are scheduled to get an X-ray of their ankle in the emergency department, to examine their ankles with an ultrasound machine as well. Since the bedside ultrasound is not significantly time-consuming, does not require patients to remain still, and is readily available in the department, the procedure will be performed while kids are waiting to get an X-ray, getting registered, or awaiting further treatment. On the data collection form, the investigators will document the patients' names, birthdates, medical record numbers so that their X-ray results can be compared to the ultrasound results for the purpose of the study. The information will be stored in a secure cabinet in a locked office. The investigators will also document which side is injured, where the patient feels pain and what the ankle looks like to help perform the ultrasound. The results of both the ultrasound and X-ray will be documented for each patient.

NCT ID: NCT01338129 Not yet recruiting - Ankle Fracture Clinical Trials

The Effect of Vitamin c on Preventing Complex Regional Pain Syndrome (CRPS Type I) Following Ankle Fracture

CRPS
Start date: April 2011
Phase: N/A
Study type: Interventional

The use of prophylactic treatment with vitamin c may prevent complex regional pain syndrome (CRPS)

NCT ID: NCT01333371 Not yet recruiting - Clinical trials for Distal Radius Fracture

Assessing Volar Locking Plates in Patients Under 65 With a Distal Radius Fracture

DRF
Start date: April 2011
Phase: N/A
Study type: Interventional

Patients will be randomized to volar plating with early ROM versus closed reduction with K-wires and 6 weeks of cast immobilization to determine if there is any advantage to volar plating in this subgroup of patients with distal radius fractures.