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Hip Fractures clinical trials

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NCT ID: NCT00937911 Completed - Clinical trials for Venous Thromboembolism

Prevention of Venous Thromboembolism in Subjects Undergoing Hip Fracture Surgery or Surgery in the Lower Extremities

Start date: June 2009
Phase: Phase 3
Study type: Interventional

The study objective is to evaluate the efficacy and safety of oral YM150 for prevention of venous thromboembolism in subjects undergoing hip fracture surgery or surgery in the lower extremities.

NCT ID: NCT00919230 Completed - Hip Fracture Clinical Trials

Randomised Trial Comparing Iron Supplementation Versus Placebo in the Treatment of Anaemia After Hip Fracture

Start date: July 2004
Phase: Phase 3
Study type: Interventional

At present our current practice is to provide a course of oral iron therapy for those patients with a post-operative haemoglobin which is below normal, but not severe enough to require a blood transfusion. Such a practice is not without side effects from the iron tablets, namely ingestion, nausea, diarrhoea, constipation. There is little evidence in the literature to support the current practice of using iron, with only one small randomised trial suggesting such therapy is unnecessary. We propose to recruit 300 patients recovering from a hip fracture with a post-operative haemoglobin below 11g/l. For those patients willing to enter the study, half will be given oral iron therapy (ferrous sulphate 200mg twice daily) for one month. The haemoglobin will be checked when the patients attends the hip fracture clinic at 6 weeks after discharge.

NCT ID: NCT00887354 Completed - Osteoporosis Clinical Trials

A Study That Will Compare the Effect of Two Drugs on Participants With Low Bone Mass and a Recent Hip Fracture

MOVE
Start date: April 2009
Phase: Phase 4
Study type: Interventional

This study will evaluate whether teriparatide is superior to the active comparator in the change from baseline of lumbar spine BMD (bone mineral density) in men and postmenopausal women with low bone mass and a recent pertrochanteric hip fracture.

NCT ID: NCT00873548 Completed - Clinical trials for Trochanteric Fractures

Treatment of Unstable Trochanteric Fractures With the Proximal Femoral Nail - Antirotation (PFNA)-Asia

Start date: November 2007
Phase:
Study type: Observational

The primary objective of this prospective multicenter study is to assess any fracture fixation complication and revision rates during the clinical use of the Proximal Femoral Nail Antirotation Asia (PFNA Asia) for the treatment of unstable trochanteric fractures.

NCT ID: NCT00848913 Completed - Hip Fracture Clinical Trials

Strength Training After Hip Fracture Surgery

Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effect of progressive strength training of the fractured limb in patients with hip fracture, during admittance in an acute orthopedic ward. The primary study hypothesis is that the training will reduce the strength deficit in the fractured limb in comparison with the non-fractured limb. Secondary, that patients following the intervention will present larger improvements in physical function compared to controls.

NCT ID: NCT00800124 Completed - Hip Fracture Clinical Trials

Study on Cemented Versus Non-cemented Hemiarthroplasty in Elderly With Hip Fractures

CNC
Start date: June 2005
Phase: N/A
Study type: Interventional

The objective is to study the overall frequency and cumulative rate (during one year) of clinical morbidity (defined as any hospitalization without fatal outcome) and mortality in all consecutive patients undergoing HF surgery (pins and prosthetic implants) and compare this to the group of patients receiving prosthetic implants and further find out if there is a difference between the non-cemented and cemented groups. Between the same prosthetic groups, the investigators want to study the overall frequency of in-hospital subclinical organ damage and dysfunction of myocardium, liver and lungs, using biochemical plasma markers. Finally, the investigators want to perform perioperative cost benefit calculations and out of hospital quality of life analysis between the surgical groups.

NCT ID: NCT00761813 Completed - Clinical trials for Femoral Neck Fractures

Using Alternative Implants for the Surgical Treatment of Hip Fractures (The FAITH Study)

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

Each year, hip fracture, an injury that can impair independence and quality of life, occurs in about 280,000 Americans and 36,000 Canadians. The annual healthcare costs associated with this injury are expected to soon reach $9.8 billion in the United States and $650 million in Canada. It is important to have in place optimal practice guidelines for the surgical handling of this injury. One type of hip fracture, called a femoral neck fracture, is often treated with a surgical procedure called internal fixation. When performing internal fixation, most orthopaedic surgeons favor using multiple small diameter screws over using a single large diameter screw with a sliding plate. However, use of the sliding hip screw might in fact result in fewer complications after surgery and reduce the need for a second surgery, called a revision surgery. This study will compare the two different surgical procedures to determine which one results in better outcomes after surgery.

NCT ID: NCT00755365 Completed - Clinical trials for Pelvic Fractures and Associated Hemodynamic Instability

Intraoperative Angioembolization in the Management of Pelvic Fracture-Related Hemodynamic Instability

Start date: January 2003
Phase:
Study type: Observational

Mortality associated with pelvic fractures resulting from blunt trauma ranges between 6 and 18%. In cases where hemodynamic instability is also present, the mortality rate is significantly greater, and has been reported as high as 60%. There is no general consensus among traumatologists as to the initial management of this complicated subgroup of patients. It is largely debated whether emergent orthopedic fixation or angiographic embolization should be the first line of treatment for pelvic hemorrhage

NCT ID: NCT00749489 Completed - Pain Clinical Trials

Improving Pain and Function in Hip Fracture

Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare two different methods of treating pain after a hip fracture.

NCT ID: NCT00746876 Completed - Hip Fractures Clinical Trials

Unipolar or Bipolar Hemiarthroplasty in the Treatment of Displaced Femoral Neck Fractures.

HEMIUNIBIPOL
Start date: September 2009
Phase: N/A
Study type: Interventional

Hemiarthroplasty of the hip is standard treatment of femoral neck fractures (hip fractures). Hemiarthroplasty means replacing the hip joint with a metal prosthesis. Unipolar prostheses has a one-piece design where the hip movement occurs between the prosthesis and the acetabulum (hip socket). A bipolar prosthesis has an additional artificial joint between the two components of the prosthesis. Both treatments are clinically proven and common around the world. No clinical trial has proven benefits of one or the other prosthesis design. The investigators want to measure the differences in acetabular wear using these two prostheses, using radiostereometric measurements.