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Fractures, Bone clinical trials

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NCT ID: NCT01144208 Completed - Clinical trials for Distal Radius Fractures

The Influence of Local Bone Status on Complications After Surgical Treatment of Distal Radius Fractures

Start date: February 2007
Phase: Phase 4
Study type: Observational

The purpose of this study is to evaluate if poor bone quality increases the risk of specific types of treatment complications in patients with distal radius fractures treated with open reduction and Locking Compression Plates(LCP).

NCT ID: NCT01143675 Completed - Clinical trials for Proximal Humeral Fractures

Influence of Local Bone Status on Complications After Surgical Treatment of Proximal Humerus Fractures

Start date: March 2007
Phase:
Study type: Observational

The purpose of this study is to evaluate if poor bone quality increases the risk of specific types of treatment complications in patients with proximal humerus fractures treated with open reduction and angle-stable plates (Proximal Humeral Internal Locking System - PHILOS).

NCT ID: NCT01139528 Completed - Clinical trials for Fractures of the Neck

Conservative or Operative Treatment of Fractures in the Neck of the 5th Metacarpal Bone

MC-studien
Start date: May 2010
Phase: N/A
Study type: Interventional

A multi-site randomized controlled trial where patients are allocated to operative treatment or conservative treatment of fractures of the neck of the 5th metacarpal bone. The study goal is to identify which degree of angular displacement in the fracture that requires operative intervention.

NCT ID: NCT01134354 Completed - Clinical trials for Tibia Fracture (Isolated)

The Role of Patient Expectations in Traumatic Orthopedic Outcomes-TEFTOM EURASIA

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

Design: Prediction trial, up to 10 sites in Asia and Europe Goal: To better understand the "success" or "failure" after orthopedic trauma surgery by developing a model that can be applied clinically as a user-friendly "baseline" questionnaire - capable of predicting "success" or "failure" based on a patient's pre-surgical expectations of their final outcome and to validate a novel outcomes measure (TOM). Primary aim: To assess the psychometric properties of predictive validity, internal consistency and reproducibility of the trauma expectation factor (TEF) in the Eurasian population. Secondary aim: To assess the psychometric properties of criterion validity, internal consistency,reproducibility, and sensitivity to change of the TOM in the Eurasian population. Key questions related to patient and surgeon expectations: - How different, or similar, are patient and surgeon expectations? - Do expectations change over time? - Do patient expectations predict outcomes in validated measures use today?

NCT ID: NCT01134094 Completed - Ankle Fractures Clinical Trials

Combined Randomised and Observational Study of Type B Ankle Fracture Treatment

CROSSBAT
Start date: August 2010
Phase: N/A
Study type: Interventional

This study will determine whether operative management confers improved short and long−term outcomes for patients with isolated AO type 44−B1 distal fibula fractures when compared with non−operative management.

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: 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: 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.