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Fractures, Bone clinical trials

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NCT ID: NCT02944058 Active, not recruiting - Shoulder Fractures Clinical Trials

Plate Fixation Versus Intramedullary Nailing of 3 and 4 Part Proximal Humerus Fractures

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

The purpose of the project is to compare the management of 3 and 4 part proximal humerus fractures (PHF) with an angular stable plate (Philos) with that of an intramedullary nail (Multiloc) in light of complications, radiological, economical, functional and clinical outcome.

NCT ID: NCT02901938 Active, not recruiting - Clinical trials for Femoral Neck Fracture

Feasibility of Implantation of Cemented Femoral Stem for Osteoporotic Femoral Neck Fracture in Elderly Patients

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

This study will investigate the effects of implantation of cemented femoral stem versus percutanous internal fixation with cannulated compression screws on hip joint function recovery, pains, femoral head collapse and sterile prosthesis loosening, peri-prosthesis infection, and the histocompatibility of prosthesis material with host tissue in the elderly patients with osteoporotic fracture of proximal femoral neck complicated by avascular necrosis of the femoral head, which will provide scientific evidence for selecting surgical methods and internal fixation/artificial prosthesis material for osteoporotic fracture of proximal femoral neck in the elderly patients.

NCT ID: NCT02880501 Active, not recruiting - Clinical trials for Intertrochanteric Femoral Fracture

Safety and Effectiveness of Proximal Femoral Nail Antirotation for the Treatment of Intertrochanteric Femoral Fracture

Start date: January 2015
Phase: N/A
Study type: Interventional

Minimally invasive PFNA fixation for the treatment of intertrochanteric femoral fracture will be used in 20 patients within 2 years to objectively validate the safety and effectiveness of PFNA in the treatment of fracture of long tube-like bone.

NCT ID: NCT02789774 Active, not recruiting - Spinal Fractures Clinical Trials

Uppsala Study on Odontoid Fracture Treatment in the Elderly

USOFT
Start date: February 2012
Phase: N/A
Study type: Interventional

A multicenter randomized controlled trial is performed in Sweden (Uppsala, Malmo and Stockholm) comparing surgery with posterior C1-C2 fusion and conservative treatment with a rigid collar. Follow up will be performed up to one year after start of treatment registering EQ5D, NDI and cervical CT scans. Mortality will be documented during follow-up. All direct and indirect costs of treatment will be registered and used for cost-effectiveness analysis.

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: NCT02627040 Active, not recruiting - Hip Fracture Clinical Trials

Intertrochanteric Femoral Fracture Fixation Trial

Start date: November 30, 2015
Phase: N/A
Study type: Interventional

The main goal of the study is to determine which cephalomedullary nail results in a better functional outcome for the patient with an unstable intertrochanteric hip fracture. Subjects will be randomized to fixation with either a Gamma3 cephalomedullary nail or an InterTan cephalomedullary nail. Outcomes will be reviewed over a 12 month follow-up period.

NCT ID: NCT02606162 Active, not recruiting - Clinical trials for Severe Fragility Fracture

Outcomes of Severe Osteoporotic Fractures Hospitalized in France: the CROSS Cohort

CROSS
Start date: June 8, 2016
Phase:
Study type: Observational

The purpose of this study is to determine the outcomes of severe osteoporotic fractures hospitalized in France, the risk of incident severe fracture at 2 years and 5 years and the risk of mortality over 2 and 5 years.

NCT ID: NCT02604589 Active, not recruiting - Rib Fractures Clinical Trials

Continuous Intercostal Nerve Blockade for Traumatic Rib Fractures

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

Rib fractures are common injuries in accident patients and can be associated with significant pain during recovery. If poorly controlled, pain from splinting due to rib fractures can result in difficulty in breathing leading to incomplete expansion of lung, and even the need to put a patient on a ventilator to help them breathe. Therefore, pain control is critical in managing patients with rib fractures. To date, many studies have shown the effectiveness of continuous intercostal nerve blockade (a slow release of pain medications at the site of injury that prevents the transmission of pain signals). This approach has never been studied in a randomized fashion in rib fracture patients, and has never been compared to patient-controlled narcotic pain medication, commonly used at many hospitals. The purpose of this study is to evaluate the effectiveness of the placement of an elastomeric infusion pump (a small, external, wearable balloon used to deliver medication over time) attached to a continuous infusion catheter or "soaker" catheter (a tube which releases the pain medication through tiny holes in it, right at the site of injury) to deliver local anesthetic medication to reduce pain caused by two or more rib fractures.

NCT ID: NCT02529267 Active, not recruiting - Fractures, Bone Clinical Trials

Prospective Abuse and Intimate Partner Violence Surgical Evaluation

PRAISE-2
Start date: August 2015
Phase:
Study type: Observational

Intimate partner violence (IPV), also known as domestic abuse, is a leading cause of non-fatal injury in women worldwide. 1 in 6 women attending surgical fracture clinics have a history of IPV in the past year. Given the high prevalence and costs associated with IPV, there is a need to identify health outcomes associated with IPV, the incidence of new and worsening cases of IPV, and resource use among IPV victims. This prospective cohort study of women with fractures and dislocations will assess differences in injury-related outcomes (time to fracture healing, injury-related complications, and return to pre-injury function) between abused and non-abused women. This study will also determine whether a musculoskeletal injury can lead to new or worsening abuse by an intimate partner and how patterns of IPV change over time following musculoskeletal injuries.Finally, the proposed study will also inform the feasibility of a larger multinational cohort study.