Clinical Trials Logo

Ulna Fractures clinical trials

View clinical trials related to Ulna Fractures.

Filter by:
  • Terminated  
  • Page 1

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: NCT01484366 Terminated - Clinical trials for Fractures of Radius and Ulna

Forearm Shaft Fractures: Plating of Radius and Ulna Versus Plating of Radius and Nailing of Ulna

Start date: September 2010
Phase: N/A
Study type: Interventional

The hypothesis is that intramedullary nailing of the ulna and plating of the radius will result in a superior outcome as evidenced by two primary end points: 1. a lower rate of implant pain 2. a lower re-operation rate to remove painful hardware.

NCT ID: NCT01397643 Terminated - Clinical trials for Olecranon Fractures in the Elderly

A Trial of Non-operative Versus Operative Management of Olecranon Fractures in the Elderly

Start date: October 2010
Phase: N/A
Study type: Interventional

Proximal forearm fractures comprise approximately 5% of all fractures, with olecranon fractures accounting for almost 20% of thes fractures. There is limited conclusive evidence regarding the optimal treatment and outcome of these fractures within the elderly population with one case series in the literature describing 13 patients. Our trial includes all patients equal to or over the age of 75yrs presenting to the Edinburgh and Fife Orthopaedic Trauma Units with an isolated olecranon fracture. Patients who consent to enrol in the trial will be randomised to operative fixation using one of two treatment methods. Patients in the nonoperative group will be place in a sling for two weeks and then allowed to mobilise under supervised physiotherapy as per normal protocol. For those patients in the operative group, tension band wire of plate fixation will be employed depending on the choice of their supervising consultant. Patients will be evaluated over a one year period following their treatment.