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Fractures, Bone clinical trials

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NCT ID: NCT02720055 Completed - Fractures, Bone Clinical Trials

Rehabilitation Workbook After Wrist Fracture.

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

A randomised controlled trial to compare two different rehabilitation work books used in patients with wrist fracture.

NCT ID: NCT02719340 Completed - Spinal Fractures Clinical Trials

Short Segment Fixation in Thoracolumbar Osteoporotic Fracture

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

Although long-segment posterior spinal fixation might provide more rigid fixation, the procedure increases perioperative morbidities in the elderly. The present study reviews the results of short-segment decompression and reconstruction in thoracolumbar fragile fractures.

NCT ID: NCT02717546 Completed - Clinical trials for Distal Tibia Fractures

Zimmer® MotionLoc® in Distal Tibia Fractures

Start date: February 2016
Phase:
Study type: Observational

The objective of this observational prospective study is to systematically document the clinical outcomes of Zimmer MotionLoc Screws for Periarticular Locking Plate System applied to distal tibia fracture treatment and confirm safety and performance of the screws.

NCT ID: NCT02714257 Completed - Fractures, Bone Clinical Trials

Working to Increase Stability Through Exercise

WISE
Start date: November 21, 2016
Phase: N/A
Study type: Interventional

The investigators propose a 36-month multi-center randomized effectiveness trial to compare the impact of an Enhanced Usual Care (Control) intervention, with Exercise Coaching (Exercise), on Fragility Fractures and Serious Fall-Related Injuries (FF/SFRI) in patients with a previous fragility fracture (FF). The investigators will also examine the impact of the intervention on several secondary outcomes like: loneliness, physical function, and bone strength. The investigators will do this by following a Pragmatic trial design: 1) limiting exclusions to increase representativeness, 2) limiting research contacts (average 30 min/year) and 3) limiting measures to those practicable for use in usual care.

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: NCT02696915 Completed - Clinical trials for Proximal Femur Fractures

Fascia Iliaca Compartment Block for Proximal-end Femur Fractures

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

Fracture femur is a common injury which is associated with excruciating pain. Positioning for neuraxial blocks is always challenging because even slight overriding of the fracture ends is intensely painful .It can causing major patient distress which accompanied by well-known physiological sequelae such as sympathetic activation causing tachycardia, hypotension, and increased cardiac work that may compromise high-risk cardiac patients. Fascia iliaca compartment block is highly effective in blocking lateral cutaneous nerve of the thigh and femoral nerve. Fascia iliaca compartment block is not only easy to perform but it is also associated with minimal risk as the local anesthetic is injected at a safe distance from the femoral artery and femoral nerve. It is always safe to perform the fascia iliaca compartment block prior to spinal anesthesia as the patient can respond during administration of the local anesthetic and can prevent intra-neuronal injections

NCT ID: NCT02693288 Completed - Postoperative Pain Clinical Trials

Comparing Efficacity of Analgesia Between Ultrasound-guided Nerve Block and Local Infiltration After Wrist Fracture Surgery

BNINF
Start date: December 2015
Phase: N/A
Study type: Interventional

Distal radial fracture reparations by volar plating are often managed under regional anaesthesia, but are associated with severe pain when the block ends. Acute post-operative pain may delay rehabilitation, and even be a risk factor for the development of chronic pain. The use of opioids and the inevitable opioid-related side effects further decrease patient satisfaction. A multimodal approach to pain management should include local or regional analgesia technique when possible. In the case of wrist fractures, two methods are available: peripheral nerve block by the anaesthesiologist or surgical site local infiltration by the surgeon with a long-acting local aesthetic. Both techniques are commonly used for the management of postoperative pain after diverse orthopaedic surgeries. The purpose of this study was to determine the equivalence between ultrasound-guided peripheral nerve block and local infiltration by the surgeon for short-term postoperative analgesia after surgical reparation of isolated closed wrist fractures by volar plating under regional anaesthesia. The quality of postoperative pain, patient satisfaction and adverse events were recorded for the first 48 hours following surgery.

NCT ID: NCT02688296 Completed - Fibula Fracture Clinical Trials

Effectiveness Of The Fibulock Intramedullary Nail

Fibulock
Start date: May 24, 2016
Phase:
Study type: Observational

The objective of this post-market clinical study is to evaluate efficacy outcomes and complication rates in patients who have received the Fibulockā„¢ Intramedullary Nail.

NCT ID: NCT02680028 Completed - Hip Fracture Clinical Trials

Short Versus Standard Intramedullary Nail for Trochanteric Hip Fractures

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

In England each year over 65,000 people fracture their hip. Most of these patients are elderly females with the fracture occurring after a simple trip or stumble. Approximately half of these fractures are classified from their relationship to the hip joint capsule as extracapsular. The majority of these fractures are treated surgically by internal fixation using, either a plate and screws (sliding hip screw) or nail and screws (intramedullary nail). Recent randomised studies from Peterborough involving 1000 patients have indicated that there are modest benefits for treating this type of fracture with an intramedullary nail in comparison to a sliding hip screw. This study aims to progress from these earlier studies to determine if a slightly thinner and shorter intramedullary nail (175mm in length), has any significant advantages or disadvantages to the standard length (220mm) intramedullary nail. Both implants to be used in this study are in routine use around the world and are being used within their licenced indication. The study is therefore using two different designs of implant within their recommended area of use, but in which there is uncertainty as to which is the best design.

NCT ID: NCT02670629 Completed - Radius Fractures Clinical Trials

Management of Distal Radius Fractures in Children Younger Than 11 Years Old.

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

This fractures have been managed with anatomical reduction performed under anesthesia or using sedatives. In our institution this means prolonged hospital stay, involvement of an anesthesiologist and the use of an special room in the Emergency Department. This research protocol was born after reports were published regarding leaving the fractures in an overriding position and cast with good functional and acceptable radiographical results; said study was observational, providing valuable but limited information about this treatment option. On the other hand, our study is a randomized controlled trial between to groups of patients younger than 11 years old who presented to the Emergency Department with completely displaced distal radius fractures, they were randomly assigned to one of two groups, either a closed anatomic reduction and short cast or a closed overriding alignment and short cast.