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Humeral Fractures 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: NCT02913378 Recruiting - Shoulder Fractures Clinical Trials

Conservative vs Surgical Treatment for Proximal Humerus Fractures in the Elderly

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

This is a randomized trial comparing conservative with surgical treatment (with open reduction and locking plate fixation) for proximal humeral fractures in patients aged more than 60 years.

NCT ID: NCT02863289 Completed - Humeral Fractures Clinical Trials

The Outcomes of Proximal Humerus Fractures in Children

Start date: October 2016
Phase:
Study type: Observational

To date, the clinical benefits and harms of surgical intervention in proximal humerus fractures in children remain debatable. The practical question raised by orthopaedic surgeons is: for children and adolescent, are the clinical and radiological outcomes after non-operative management as equivalent as after surgical management for proximal humerus fractures? The investigators' hypothesis is that due to the healing potential of the proximal humerus, the outcome from this fracture is usually excellent. The investigators have applied for Caldicott approval to identify a cohort of eligible patient from NHS Tayside's radiography service. With the community health index (CHI) number, the investigators can review all shoulder X-rays performed in children and adolescents, aged from 10 to 18-year-old in NHS Tayside, from 2008 to 2015. The Caldicott approval also allowed the investigators to obtain clinical communication from the Clinical Portal (electronic summary healthcare records). The investigators will then conduct mail questionnaires, based on the Upper Extremities Functional Index (UEFI). The investigators will send out invitation letter with participation information and the UEFI questionnaires to the eligible patients; with return postages. If no response within 2 weeks, the investigators will send out 1 further reminder. If no further response, the patient will be excluded from the study.

NCT ID: NCT02861495 Terminated - Humeral Fractures Clinical Trials

Humeral Compression/Distraction Device

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

The proposed study of humeral shaft fractures in adults will examine outcomes in patients treated with the Humeral Trauma Nail System to treat displaced humeral shaft fractures (displaced OTA code 12A, B, or C), nonunions, or malunions. The device to be studied uses an internal gear system controlled wirelessly by rare earth magnets, which typically offers distraction for lengthening. In the humerus however, during the treatment of acute fractures, this percutaneously inserted nail can also offer compression during the healing process, thereby negating the effect of gravity, which may in turn lead to a faster and more consistent rate of union. Furthermore, in cases of slower healing the dynamic properties of the nail may employ an "accordion technique" (alternating compression-distraction, a feature unique to this implant.

NCT ID: NCT02826538 Terminated - Fracture of Femur Clinical Trials

3D Geplante Osteosynthesen Mit Patientenspezifischen Zielvorrichtungen

Start date: July 30, 2017
Phase: N/A
Study type: Interventional

Goal of this study is to evaluate the accuracy of 3D computer-planned fracture fixation with patient-specific instruments for clavicle, upper extremity, lower extremity and pelvis fractures compared with the standard procedure of fracture fixation.

NCT ID: NCT02803177 Completed - Clinical trials for Humerus Fracture Displaced Proximal

Cell Therapy by Autologous BMC for Large Bone Defect Repair

BMC2012
Start date: July 2, 2016
Phase: Phase 2
Study type: Interventional

In the present phase-II clinical trial the researchers investigate efficacy and proof of concept of the augmentation with preoperatively isolated autologous BMC cells seeded onto ß-TCP in combination with an angle stable fixation (Philos plate®) for the therapy of proximal humeral fractures.

NCT ID: NCT02784522 Completed - Humerus Fractures Clinical Trials

Minimally Invasive of Proximal Humerus Fractures With Internal Fixation Improves Shoulder Function in Older Patients

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

This study protocol represents an attempt to objectively choose appropriate methods for internal fixation of proximal humerus fractures in older patients by comparing locking compression plate with conventional steel plate fixation to improve shoulder function.

NCT ID: NCT02756156 Not yet recruiting - Humerus Fracture Clinical Trials

Low Dose Interscalene and Infraclavicular Block for Humerus Surgery

Start date: April 2016
Phase: N/A
Study type: Observational

Combining interscalene block with infraclavicular block for humerus surgery provides a unique surgical anaesthesia and postoperative analgesia.

NCT ID: NCT02733666 Completed - Humeral Fractures Clinical Trials

Internal Fixation of Lateral Humeral Condyle Fractures With Absorbable Screws in Children

Start date: May 2007
Phase: Phase 1
Study type: Interventional

Lateral humeral condyle fractures are the second most common elbow fractures in children. Displaced and rotated fractures require stabilization and reduction. Kirschner wires (K-wires) are most commonly used for fracture fixation. Here, the investigators introduce a new fixation method involving absorbable screws. The investigators aimed to determine if it is feasible to treat lateral humeral condyle fractures with absorbable screws by comparing the functional outcomes obtained using screw fixation vs. K-wire fixation.

NCT ID: NCT02656628 Withdrawn - Clinical trials for Diaphyseal, Distal or Proximal Tibia Fracture

Observational Patient Registry of the Dynamic Locking Screws

DLS
Start date: May 2015
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this multi-center patient registry is to obtain first clinical results and to assess short and mid-term clinical outcome data of patients treated with DLS.