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Femoral Neck Fractures clinical trials

View clinical trials related to Femoral Neck Fractures.

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NCT ID: NCT02803983 Completed - Clinical trials for Femoral Neck Fractures

Pediatric Hip Plate Versus Cannulated Screw in Pediatric Femoral Neck Fracture

PFNF
Start date: June 2016
Phase: N/A
Study type: Observational

The purpose of this study is to compare the early postoperative radiologic and clinical outcomes of pediatric hip plate and cannulated screw fixation in pediatric femoral neck fracture (Delbet type II and Delbet type III).

NCT ID: NCT02783274 Recruiting - Clinical trials for Rheumatoid Arthritis

Actis Total Hip System 2 Year Follow-up

Actis14014
Start date: July 1, 2016
Phase: N/A
Study type: Interventional

Two-year (2 year) information regarding the performance of the commercially available Actis™ Total Hip System in order to obtain and evaluate the clinical outcomes on a series of cementless primary total hip arthroplasty (THA) and hemi-hip arthroplasty procedures using clinical, radiographic and device and procedure related adverse event assessments.

NCT ID: NCT02780076 Active, not recruiting - Clinical trials for Femoral Neck Fractures

Recovery of Physical Functioning After Hip Fracture

HIPFRAC
Start date: May 30, 2016
Phase: N/A
Study type: Interventional

The survivors after hip fracture often report severe pain and loss of physical functioning. The poor outcomes cause negative impact on the person's physical functioning and quality of life and put a financial burden on society. It is important to continue and progress the functional training that already started at the hospital, while the patients are transferred to short-term stays in a nursing home before they are returning to home. The aim presently is to examine the effects of a functional training program by a RCT design, initiated by the physiotherapist and performed by the nurses, on physical functioning while the patients are at short term stays in primary health care.

NCT ID: NCT02776631 Active, not recruiting - Clinical trials for Femoral Neck Fractures

Pinloc Versus Hansson Pins in the Treatment of Femoral Neck Fractures.

Start date: May 2014
Phase: N/A
Study type: Interventional

A prospective randomized study comparing a new implant with three interlocked pins for internal fixation of femoral neck fractures (Hansson Pinloc System, Swemac Linköping, Sweden) versus 2 parallel pins with hooks (Hansson Pins, Swemac Linköping, Sweden).

NCT ID: NCT02771639 Completed - Infection Clinical Trials

Early Periprosthetic Joint Infection and Outcome Debridement, Antibiotics and Implant Retention

DAIR
Start date: January 2016
Phase: N/A
Study type: Observational

Introduction Periprosthetic joint infection (PJI) is a severe complication to hip arthroplasty for femoral neck fractures (FNF). Debridement, antibiotics and implant retention (DAIR) is recommended in early PJI in association with stable implants. Few studies have evaluated the outcome of DAIR in this fragile population.The purpose of this study was to analyze risk factors for PJI and the short-term outcome of DAIR in FNF patients treated with a hip arthroplasty. Methods A consecutive series of patients had been treated with either a total hip arthroplasty or a hemi hip arthroplasty for a displaced FNF at our institution. Data were retrospective analysed.

NCT ID: NCT02699619 Completed - Hip Fractures Clinical Trials

Undisplaced Femoral Neck Fractures 2 Hansson Pins or 3 Pins Interlocked in Plate (Pinloc) Using RSA

Start date: March 2016
Phase: N/A
Study type: Interventional

Femoral neck fractures represent about half of the hip fractures and are further divided into displaced and undisplaced fractures. Displaced femoral neck fractures are almost always treated surgically with arthroplasty. However there is an ongoing debate on which implant is superior for undisplaced fractures. A novel implant design (Pinloc) has been developed by Swemac Innovation AB. While the original implant consisted of 2 isolated hook pins, the modified design consists of 3 titanium hook pins interlocked in an aluminum plate. Interlocking is a new principle of implant design and improves fixation and load transfer amongst the pins. The superiority of the modified design is so far only proven preclinically. The role of the Pinloc in clinical use remains unclear. Investigators are planning a randomized controlled trial on undisplaced femoral neck fractures to establish a method for implanting the tantalum markers, to observe the fracture healing process and to further investigate the role of the Pinloc.

NCT ID: NCT02664909 Completed - Clinical trials for Femoral Neck Fractures

Topical (Intra-Articular) Tranexamic Acid and Transfusion Rates Following Hip Hemiarthroplasty

Start date: January 1, 2016
Phase: Phase 4
Study type: Interventional

This study is a double-blinded placebo-controlled clinical trial evaluating the efficacy of 1 gram of topically applied tranexamic acid vs. saline placebo for the reduction of transfusion following hip hemiarthroplasty surgery.

NCT ID: NCT02630836 Withdrawn - Clinical trials for Femoral Neck Fracture

Allogeneic Mesenchymal Stromal Cells in Elderly Patients With Hip Fracture

Start date: December 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Prospective, unicenter, randomized, open-label, single-dose, two-arms blinded assessor pilot study. Thirty-two (32) elderly patients with hip fracture will be randomized to one of the two treatment-arms (Xcel-MT-osteo-beta or Standard treatment) and be followed for 12 month with the primary objective of safety. Secondary objectives are efficacy through axial tomography and xRay, clinical efficacy and quality of life questionnaire.

NCT ID: NCT02629484 Completed - Hip Fractures Clinical Trials

Trial of Focused Cardiac Ultrasound for Fractured Neck of Femur Surgery

ECHONOFII
Start date: February 1, 2016
Phase: N/A
Study type: Interventional

Hip fracture surgery is a major world health care burden and concern, as it has a large and increasing prevalence and carries very high patient mortality, disability and community health care cost. As the commonest cause of mortality is from cardiac complications, and cardiac disease is prevalent and frequently missed by standard care, we hypothesise that earlier and more accurate diagnosis and treatment of cardiac pathology in this cohort will lead to improved outcome. Focused cardiac ultrasound (FCU) is a new increasingly popular technique used by doctors that enables earlier and more accurate diagnosis of cardiac disorders that can be performed routinely before hip fracture surgery. Our preliminary data of 64 patients demonstrated that routine FCU before surgery lead to a change in cardiac diagnosis and management in 50% of patients requiring hip fracture surgery, which was associated with a 50% reduction in mortality 12 months after surgery compared with controls. It is therefore important for a large randomised trial to be performed to confirm or rebuke these findings, as if true, would have a very large impact on health care and may also improve health care and outcome in other high-risk surgical populations. The proposed pilot study is a pilot study which aims to establish feasibility, safety, compliance and group separation prior to commencing a definitive multicentre trial.

NCT ID: NCT02591342 Completed - Hip Fracture Clinical Trials

Comparison of a Cemented, Polished Tapered Stem and an Anatomic Stem for Femoral Neck Fracture

Start date: September 2009
Phase: N/A
Study type: Observational

Postoperative periprosthetic femoral fracture after hip arthroplasty is associated with considerable morbidity and mortality. Recent cohort studies have demonstrated a high incidence of PPF in elderly patients treated with two commonly used polished, tapered, collarless stems in elderly patients. The aim of this study was to compare the rate and characteristics of PPF in a consecutive cohort of patients treated either the polished tapered CTP stem or the matte anatomic SP2 stem in an elderly population above 80 years of age with femoral neck fracture.