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Humeral Fractures clinical trials

View clinical trials related to Humeral Fractures.

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NCT ID: NCT00698867 Completed - Clinical trials for Rheumatoid Arthritis

A Clinical Investigation of the Discovery™ Elbow System

Start date: June 2002
Phase: N/A
Study type: Observational

The purpose of this study is to perform a five-year, multi-center prospective evaluation of the Discovery™ Elbow System for outcome and durability. Relief of pain and restoration of function will determine long-term clinical outcome while durability will be measured by the absence of revisions.

NCT ID: NCT00698750 Terminated - Clinical trials for Rheumatoid Arthritis

A Clinical Investigation of the Copeland™ Humeral Resurfacing Head

Start date: April 2004
Phase: N/A
Study type: Observational

The purpose of this study is to perform a five-year, prospective evaluation of the Copeland™ Humeral Resurfacing Head Prosthesis for outcome and durability. Relief of pain and restoration of function will determine long-term clinical outcome while durability will be measured by the absence of revisions.

NCT ID: NCT00612391 Completed - Clinical trials for Closed Fracture Proximal Humerus, Neck

Lateral Mini Approach vs Anterior Approach for Plating of Proximal Humerus Fracture

HURA
Start date: November 2007
Phase: N/A
Study type: Interventional

A prospective randomized clinical trial is proposed to compare the plate fixation of proximal humerus fractures using a minimally invasive lateral approach and the traditional anterior approach.Forty five patients will be assigned to each approach (total of 90 patients) and will be assessed 7 times over a two-year period. The trial's primary objectives will be to demonstrate the efficacy of the plating technique in terms of speed of recuperation of function. The Quick DASH will be used for evaluation of function.The study will also examine secondary end-points of pain, range of motion, esthetic satisfaction and radiographic outcome, as assessed by the components of the Constant Score3,4, SF-12V2 Questionnaire, and Patient Scare Assessment Scale Questionnaire. Furthermore, the assessment of safety will be based on the rates of all reported complications and adverse events at 2 years

NCT ID: NCT00438633 Completed - Clinical trials for Proximal Humeral Fractures

Comparison of Early and Late Therapy for Adults With Non-Operatively Treated Proximal Humerus Fractures

Start date: February 2005
Phase:
Study type: Observational

The purpose of the study is to compare two common ways of rehabilitating after proximal humerus fractures treated non-operatively.

NCT ID: NCT00358787 Completed - Humeral Fractures Clinical Trials

Management of Displaced Supracondylar Fractures of the Humerus Using Lateral vs. Crossed K-wires

Start date: July 2008
Phase: N/A
Study type: Interventional

Completely displaced (Type III) supracondylar fractures of the humerus are treated in the operating room and are held together with pins stuck into the bone. There are two ways of inserting the pins: crossed and laterally. The crossed method is often used because it is thought to be more stable, but this method also carries a risk of hitting the ulnar nerve. It is not known which method is more stable. Our hypothesis is that loss of reduction will be equivalent between the two pinning methods.

NCT ID: NCT00326794 Terminated - Shoulder Fracture Clinical Trials

Efficacy of Shoulder Mobilisation Versus Conventional Immobilisation for Nonsurgically Proximal Humerus Fracture

Start date: October 2002
Phase: Phase 3
Study type: Interventional

Background: Nonsurgical proximal humerus fracture is common, causing prolonged disability, for which the time to begin rehabilitation is not well determined. We assessed the feasibility and efficacy of early (within 3 days’after fracture) mobilisation of the shoulder compared with conventional 3-week immobilization followed by physiotherapy.

NCT ID: NCT00240396 Withdrawn - Femur Fracture Clinical Trials

Bimodal Analgesia as Form of Pain Control Post Long Bone Fracture

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this prospective randomized study is to evaluate the risks and benefits of using bimodal analgesia, (i.e. Narcotics and NSAIDS) vs Narcotics alone post long bone fracture.

NCT ID: NCT00205959 Completed - Clinical trials for Proximal Humeral Fracture

LPHP-Philos-PHN Conservative Treatment

Start date: August 2002
Phase: Phase 4
Study type: Interventional

The aim of the study is to compare the results regarding fracture healing and functional outcome after the treatment of proximal humeral fractures with the four different treatment methods after 12w./6months and 12 months based on radiological evaluation as well as the "constant score" and the "neer score".