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Humeral Fractures clinical trials

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NCT ID: NCT02640027 Completed - Humeral Fractures Clinical Trials

The Use of Telemedicine Tool in Supracondylar Humerus Fractures in Children

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

Fractures of the supracondylar region of the humerus are among the most common pediatric injuries requiring the attention of an orthopaedic surgeon. Children with non-displaced fractures (Type I), as well as those with history of elbow trauma, have been traditionally managed with non-surgical immobilization. Recently published clinical guidelines support such practice, based on the result of two prospective studies in which either collar and cuff or posterior splint immobilization were used. When compared to collar and cuff immobilization, posterior splints resulted in better pain relief within the first two weeks of injury; however, critical outcomes, including the incidence of cubitus varus, hyperextension, and loss of reduction, were not reported. While posterior splints appear to be an attractive option for the treatment of non-displaced pediatric elbow fractures, a recent retrospective analysis on the use of posterior splints for the treatment of such injuries reported a small proportion of fractures demonstrating displacement. The potential for non-compliance with the use of removable devices, especially in the older pediatric population, is also a concern. The use of a removable immobilization that can reliably maintain fracture alignment, minimize the risk of non-compliance, and result in similar outcomes as those obtained with regular casting could be advantageous: It appears that such immobilization could be removed easily and safely at home, potentially resulting in a lower number of patient visits, decreased health-care costs, and higher patient/parent satisfaction. Telemedicine, defined as the use of telecommunication and information technologies in order to provide clinical health care at a distance, has been seldom used in the field of pediatric orthopaedics. Commonly mentioned attributes of telemedicine include improved access to healthcare providers, cost containment and increased healthcare efficiency, quality care improvements related to patient satisfaction, and potential reduction in travel time for patients and families. The purpose of this randomized, controlled, prospective study is to assess telemedicine as a tool for the treatment follow-up of non-displaced SCHF fractures in children. Investigators hypothesize that using telemedicine will result in comparable clinical outcomes as those obtained in patients treated in a clinical facility, with increased patient satisfaction and decreased healthcare costs.

NCT ID: NCT02608801 Completed - Hip Fractures Clinical Trials

Prediction and Secondary Prevention of Fractures

NOFRACTsub
Start date: April 2015
Phase:
Study type: Observational

The purpose of this study is to investigate patient related factors that contribute to increased risk of recurrent fractures and to investigate patient adherence to prescribed anti-osteoporotic drugs.

NCT ID: NCT02597972 Terminated - Clinical trials for Closed Fracture Proximal Humerus, Four Part

Reverse Total Shoulder Arthroplasty Versus Open Reduction Internal Fixation of 3&4 Part Proximal Humerus Fractures

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

Will patients who suffer complex humerus fractures have better functional outcomes and less implant failure with shoulder replacement (reverse total shoulder arthroplasty, RTSA) compared to shoulder repair (open reduction and internal fixation, ORIF)?

NCT ID: NCT02566018 Completed - Humeral Fractures Clinical Trials

Treatment of Proximal Humerus Fractures in the Elderly

prox_hum
Start date: May 1, 2015
Phase:
Study type: Observational

This study is set to evaluate a proposed standard for the treatment of proximal humerus fractures

NCT ID: NCT02524314 Active, not recruiting - Clinical trials for Acute Humerus Fractures

Safety and Efficacy Study of the Treatment of Humerus Fractures - Germany

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

The purpose of this study is to collect safety and performance data on the use of the Photodynamic Bone Stabilization System (PBSS) when used to provide stabilization and alignment for the treatment of acute humerus fractures.

NCT ID: NCT02467803 Not yet recruiting - Humeral Fracture Clinical Trials

Shoulder Functional Outcomes of Patients With Proximal Humerus Fractures: Comparison of Two Different Treatment Protocol

Start date: June 2015
Phase: Phase 0
Study type: Interventional

Fractures of the proximal humerus and the humeral head are most common injuries and the management is challenging. Functional therapy with short immobilization, followed by an accelerated physiotherapy protocol, is a simple, convenient, noninvasive, and efficient management option. This prospective randomized study is aim to assess the function of the upper extremity of patients who will be assigned to nonoperative treatment of a proximal humeral fracture. The primary objective is the Constant score. Secondary objectives are the Disabilities of the Arm, Shoulder, and Hand (DASH) instrument, measurement of shoulder range of motion (ROM), pain and depression level with Beck Depression Scale.

NCT ID: NCT02425267 Completed - Clinical trials for Humeral Fractures, Proximal

Effectiveness of a Home Telerehabilitation Program for People With Proximal Humerus Fracture

TeleFracture
Start date: June 2015
Phase: N/A
Study type: Interventional

The main objective of the study is to compare the clinical effects of the innovative telerehabilitation approach (TELE group) compared to face-to-face visits to a clinic (CLINIC group) for patients treated for a proximal humerus fracture.

NCT ID: NCT02418260 Recruiting - Humerus Fracture Clinical Trials

Surgical Interventions for the Treatment of Humeral Shaft Fractures

Start date: June 2014
Phase: Phase 3
Study type: Interventional

This study intends to determine the best surgical treatment for humeral shaft fractures. One third of the patients will be treated with open reduction and internal fixation with plate; one third, with bridge plate technique and the remaining third with locked intramedullary nail.

NCT ID: NCT02394080 Active, not recruiting - Clinical trials for Acute Humerus Fractures

Safety and Efficacy Study of the Treatment of Humerus Fractures

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

The purpose of this study is to collect safety and performance data on the use of the Photodynamic Bone Stabilization System (PBSS) when used to provide stabilization and alignment for the treatment of acute humerus fractures.

NCT ID: NCT02362100 Terminated - Clinical trials for Proximal Humerus Fracture

Proximal Humerus Fractures Randomized Control Trial

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

The primary objective is to determine if a difference exists in functional outcomes, as measured by the Constant score, when comparing nonoperative management and locking plate surgical fixation of low-energy displaced proximal humerus fractures in the elderly population over a 2-year follow-up period. Secondary outcomes will include an assessment of the ASES score, the SF-36 quality of life score, complication rates, re-operation rates, radiographic time to union, radiographic malunion, hardware position and evidence of avascular necrosis or posttraumatic osteoarthritis .