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Ulna Fractures clinical trials

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NCT ID: NCT03280602 Active, not recruiting - Olecranon Fracture Clinical Trials

Operative Treatment of Olecranon Fractures

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

The incidence of olecranon fractures is 12 per 100.000. Traditionally, isolated olecranon fractures have been treated with tension band wiring (TBW). There is a trend towards increased use of plate fixation, though TBW has yielded good and comparable patient reported outcomes. The latter method is substantially cost-effective, but higher complication reports have been reported. There are only two randomized controlled trials comparing TBW and plate fixation, and the literature is inconclusive in which fixation method is preferable in the treatment of olecranon fractures. In this multi-center trial, adult patients (18-75 years) with isolated olecranon fractures will be randomized to either TBW or plate fixation.

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: NCT02630290 Completed - Hand Injuries Clinical Trials

Addition of Dexmedetomidine to Ropivacaine-induced Supraclavicular Block (ADRIB Trial)

ADRIB
Start date: December 2015
Phase: Phase 4
Study type: Interventional

Dexmedetomidine, an alpha 2-adrenoreceptor agonist, has been found to exerts an excellent influences on the filed of perineural block. It could shorten the onset time and prolong the duration of the nerve block and improved postoperative pain. However, Dexmedetomidine-induced bradycardia or hypotension has recently attracted considerable attention because of potentially grave consequences, including sinus arrest and refractory cardiogenic shock. A low dose may help minimize cardiovascular risks associated with dexmedetomidine. However, few studies have addressed the clinical effects of low-dose dexmedetomidine as an perineural adjuvant. The present study was designed to test the hypothesis that low-dose dexmedetomidine added to ropivacaine would safely enhance the duration of analgesia without adverse effects when compared with ropivacaine alone. Investigators will conduct a single-center, prospective, randomized, triple-blind, controlled trial in patients undergoing elective forearm and hand surgery under ultrasound-guided supraclavicular brachial plexus block using either ropivacaine or ropivacaine plus low-dose dexmedetomidine. The primary outcome is self-reported duration of analgesia . Secondary outcomes include onset time and duration of motor and sensory block, total postoperative analgesics, and safety assessment (adverse effects and postoperative abnormal sensation).

NCT ID: NCT02312128 Completed - Clinical trials for Closed Fracture of Lower End of Radius and Ulna

Early Mobilization of Operatively Stabilized Distal Radius Fractures - a Randomized Controlled Trail

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

The purpose of this study is to evaluate if an early mobilization after distal radius fractures treated by surgery leads to an better functional outcome then immobilization after surgery for 5 weeks in a cast

NCT ID: NCT01752452 Completed - Clinical trials for Fracture of Distal End of Radius

Effect of Ulnar Styloid Fracture on the Outcome of Distal Radial Fractures Treated With External Fixation

Start date: January 2009
Phase: N/A
Study type: Observational [Patient Registry]

Untreated ulnar styloid fracture may affect the outcomes of distal radial fracture patient treated with external 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.

NCT ID: NCT01391936 Completed - Clinical trials for Displaced Olecranon Fractures

A Trial of Plate Fixation Versus Tension Band Wire for Olecranon Fractures

Start date: September 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 with only one prospective randomized trial (1992) in the literature comparing tension band wire and plate fixation for displaced olecranon fracture. Our trial includes all patients under the age of 75yrs presenting to the Edinburgh Orthopaedic Trauma Unit with an isolated olecranon fracture requiring operative intervention. Patients who consent to enrol in the trial will be randomised to operative fixation using one of two recognised fixation techniques - tension band wire fixation or plate fixation. Patients will be evaluated over a one year period following their surgery.

NCT ID: NCT01123447 Active, not recruiting - Surgery Clinical Trials

Surgical Treatment Versus Non-surgical Treatment of Ulnar Fractures

Start date: July 2, 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if surgery using a plate and screws to fix a forearm fracture (ulnar shaft) will improve functional outcome compared to non-operative treatment out to 1 year of follow-up. It is hypothesized that in skeletally mature patients with isolated ulnar shaft fractures, the patients treated with surgery will have improved functional outcomes compared to non-surgical treatment with below-elbow cast at 1-year follow-up. This will be measured by the Disabilities of the Arm, Shoulder and Hand (DASH) scores. Secondary outcomes will include SF-36, range of motion, pain, grip strength, return to work, and time to union.