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Fractures, Bone clinical trials

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NCT ID: NCT01133769 Withdrawn - Clavicle Fracture Clinical Trials

Operative Versus Non-Operative Treatment of Clavicle Fracture in PolyTrauma

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

About 90% of chest injuries in America are due to blunt forces, mostly as a result of motor vehicle collisions and falls. Severity varies from minor bruising to severe chest injuries. For several years, clavicle ("collarbone") fractures have been treated without surgery (non-operatively), even when the fracture is out of place (displaced). Over the last few years, however, treatment has changed more towards surgical fixation (operative), because of the sometimes difficult healing in clavicle fractures that are displaced. Several research studies have shown that cases in which the clavicle fracture never heals completely (non-union) are more frequent after nonoperative treatment, compared to operative fixation. In those cases, surgery is still required, only later (secondary surgery). Further, clavicle malunion, in which the fracture heals but is still out of place) has been shown to be high after nonoperative treatment. Recent published research studies have shown better function, higher patient satisfaction, earlier return to activity (use of the arm) and decreased nonunion and malunion following surgery, also called open reduction/internal fixation. Despite recent published research, there is still a lack of agreement on when surgical fixation should be performed for clavicle fractures. Patients with chest injuries often have clavicle fractures. Chest injuries can restrict patients' ability to breathe, cough, stand, walk and leave the hospital. Although it is unusual that chest injuries can be improved with surgery, patients with clavicle fractures and chest injuries might recover faster if the clavicle fractures were repaired. Patients are being asked to take part in the study they have sustained a clavicle fracture associated with a chest injury with or without any other injury to the abdomen, or arms or legs. The aim of this study is to determine the difference in the hospital length of stay, intensive care unit length of stay, respiratory rehabilitation (recovery of good respiratory function), functional outcome, ability to become mobile again, complications and risk of dying in trauma patients with chest injury and clavicle fracture treated operatively versus non-operatively.

NCT ID: NCT01132508 Completed - Tibial Fractures Clinical Trials

Use of a Reinforced Injectable Calcium Phosphate Bone Cement in the Treatment of Tibial Plateau Fractures

Start date: September 2008
Phase: N/A
Study type: Observational

Case series of tibial plateau fractures using Norian Drillable.

NCT ID: NCT01128868 Completed - Clinical trials for Reverse Oblique Subtrochanteric Fractures

Proximal Femur Locking Compression Plates Versus Trochanteric Nails

Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the abductor muscle strength measured with a dynamometer in patients with reverse oblique inter- or subtrochanteric fractures treated either with a proximal femur locking plate or a trochanteric nail. "Proximal femur locking plates" stands for both the PF-LCP (Synthes) and the PeriLoc (Smith & Nephew). Trochanteric nails allowed in this study are the Proximal Femoral Nail Antirotation (PFNA), the Titanium Trochanteric Fixation Nail (TFN) and the Gamma Nail (GN).

NCT ID: NCT01127776 Recruiting - Clinical trials for Bi-trimalleolar Fracture of Ankle

Bi-trimalleolar Fracture and APOS System Treatment

APOS-IL 001
Start date: October 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate of functional tests and clinical findings with APOS System treatment in patient after bi-trimalleolar fracture of ankle. These functional changes will be evaluated AOFS, FAOS, SF36 and WOMAC scores, walking laboratory GAITRite and clinical examination.

NCT ID: NCT01126398 Completed - Ankle Fracture Clinical Trials

Trauma Expectation Factor Trauma Outcome Measure

Start date: February 2007
Phase:
Study type: Observational

This study is designed as a prediction trial. That is, our primary purpose is to develop a model that can be applied clinically as a user-friendly "baseline" questionnaire that is capable of predicting "success" or "failure" based on a patient's pre-surgical expectations of their final outcome. In the process, a secondary goal is to develop an outcomes measure.

NCT ID: NCT01123512 Completed - Spinal Fractures Clinical Trials

The Kiva® System as a Vertebral Augmentation Treatment

KAST
Start date: July 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the Kiva VCF Treatment system in comparison to balloon kyphoplasty for the treatment of osteoporotic vertebral compression fractures of the thoracic or lumbar spine.

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.

NCT ID: NCT01123421 Completed - Aging Clinical Trials

Develop and Validate Ultrasonic Device for Osteoporotic Fracture Risk Assessment

BUSS03
Start date: May 2010
Phase: N/A
Study type: Observational

Study to demonstrate that the Bone UltraSonic Scanner (BUSS) can aid in detection of osteoporosis and predict prevalent osteoporotic fractures. Measurements derived from the BUSS parameters will be able to discriminate between postmenopausal women with osteoporotic fractures when compared to matched controls without history of osteoporotic fracture.

NCT ID: NCT01122628 Completed - Clinical trials for Distal Radial Fractures Treated With a DVR-A Locking Plate

Long Term Follow up of the DVR-A Locking Plate

Start date: May 2010
Phase:
Study type: Observational

The surgical treatment of wrist fractures (distal radius bone) has been changed by the introduction of a new plate design, the locking plate. This results in improved fixation and stabilisation of the fracture fragments allowing early movement. This type of plate has been increasingly used throughout the world but questions have been raised regarding the potential complications of the surgery, particularly nerve and tendon injury. The Norfolk and Norwich Hospital has treated over 250 distal radial fractures with this type of plate. The investigators plan to recall these patients to asses their long term function, general satisfaction and radiological results.

NCT ID: NCT01121159 Completed - Clinical trials for Orbital Floor Fracture

Prospective Multicenter Trial to Compare Preformed vs Non Preformed Orbital Implants

Orbita 3
Start date: June 2010
Phase:
Study type: Observational

Accuracy of posttraumatic orbital reconstruction of the medial orbital wall and/or floor is better with preoperatively preformed orbital implants than with non-preformed orbital implants.