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Multiple Trauma clinical trials

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NCT ID: NCT01938768 Completed - Mortality Clinical Trials

Effects of an Early Prehospital Administration of Tranexamic Acid on Hyperfibrinolysis in Multiple Trauma

Start date: November 2013
Phase: N/A
Study type: Observational

Severe external and internal bleedings are common in multiple trauma patients. Uncontrollable blood loss is the cause for about one third of all trauma deaths. A number of blood clotting mechanisms are known to be triggered by major blood losses. These mechanisms shall secure the organisms from loosing even more blood. To avoid an overshooting clotting behavior, inhibiting mechanisms occur as well. An important inhibiting (or fibrinolytic) mechanism is the fibrinolysis that is based on the conversion of plasminogen to plasmin. In severe bleeding situations this mechanism tends to overshoot and therewith contributes to the severity of the bleeding. This phenomena is called hyperfibrinolysis and is found in approximately one third of all multiple trauma patients. Mortality rates are increased in these patients. Tranexamic acid is an antifibrinolytic drug that inhibits the conversion from plasminogen to plasmin and therefore is able to limit the effects hyperfibrinolysis. A large study showed positive influence of tranexamic acid on mortality rates and blood loss in severely injured patients, when it was administered in an early clinical setting. In this study we want to answer the question wether a hyperfibrinolysis can be seen in an early prehospital (on the scene) setting and how it is influenced by an early prehospital administration of tranexamic acid.

NCT ID: NCT01858675 Completed - Renal Insufficiency Clinical Trials

Biomarkers Correlation With Volemia

ENVOL
Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the Biomarkers (pro adrenomedullin (MR proADM), pro arginin vasopressin (CT proAVP), pro atrial natriuretic peptid (MR proANP), Pro Endothelin) changes at Day 2, Day 5 and Day 7 of ICU admission are correlated with Intravascular volume assessed by Cr 51 on red blood cells (Day 2 and Day 7) and by I 125 on albumine Day 7. The correlation of these Biomarkers are also evaluted with other markers such as erythropoietin and catecholamines. 80 ICU patients are included.

NCT ID: NCT01669577 Completed - Multiple Trauma Clinical Trials

Independent Predictors of Mortality in Polytrauma Patients

Start date: October 2010
Phase: Phase 3
Study type: Observational

Prospective observational trial searching for independent predictors of mortality. Data was collected at trauma scene, ER, three and 24 hours of hospital stay.The patients will be followed for 30 days after hospital admission.

NCT ID: NCT01523626 Completed - Clinical trials for Multiple Trauma/Injuries

A Multicenter, Randomized Study of Early Assessment by CT Scanning in Severely Injured Trauma Patients

REACT-2
Start date: April 2011
Phase: N/A
Study type: Interventional

Computed tomography (CT) scanning has become essential in the early diagnostic phase of trauma care because of its high diagnostic accuracy. The introduction of multi-slice CT scanners and infrastructural improvements made 'total body' CT scanning (TBCT) technically feasible and its usage is currently becoming common practice in several trauma centers. However, literature provides limited evidence whether immediate 'total body' CT scanning leads to better clinical outcome then conventional radiographic imaging supplemented with selective CT scanning in trauma patients. The aim of the REACT-2 trial is to determine the value of immediate TBCT scanning in trauma patients. The investigators hypothesize that immediate 'total body' CT scanning during the primary survey of severely injured trauma patients has positive effects on patient outcome compared with standard conventional ATLS based radiological imaging supplemented with selective CT scanning.

NCT ID: NCT01373996 Completed - Atrial Fibrillation Clinical Trials

Clinical Investigation of Wireless Transmission of Invasive Blood Pressure Signal

Start date: June 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether wireless transmission of invasive arterial blood pressure signal (by HMW 10 Wireless System) from patient to patient's bedside monitor is feasible, safe and as accurate as conventional cable connection.

NCT ID: NCT01270854 Completed - Wounds and Injuries Clinical Trials

Normal Saline Versus Plasmalyte in Initial Resuscitation of Trauma Patients

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

The purpose of this study is to determine whether an intravenous salt solution called "Plasmalyte" causes less abnormality of the body's acid levels than a solution called "Normal Saline."

NCT ID: NCT01193686 Completed - Polytrauma Clinical Trials

Peer Visitation for OEF/OIF Veterans

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

The goal of this study was to train OIF/OIF Veterans with multiple injuries to be Peer Visitors, i.e., Volunteers who visit more recently OIF/OEF Veterans and provide support. We evaluated the effectiveness of the training, and any benefits that Volunteer Peer Visitors and the Recipients of Peer Visitors experienced as a result of participating in Peer Visitation.

NCT ID: NCT00872690 Completed - Brain Injuries Clinical Trials

Factors Affecting Return to Work Among OEF/OIF Veterans With Polytrauma

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

The goal of this study is to examine things that make it easy or hard for OEF/OIF veterans with polytrauma to live independently or do things "on their own" at home and in the community.

NCT ID: NCT00772213 Completed - Clinical trials for Involved Staff Member's Evaluation

The Multifunctional Image Guided Therapy Suite (MIGTS) in Emergency Multiple Trauma Care

MIGTS
Start date: February 2003
Phase: N/A
Study type: Interventional

Controlled clinical intervention study comparing the treatment of multiple trauma patients in a newly developed combined diagnostic and operation room, the multifunctional image guided therapy suite (MIGTS) versus controls. The MIGTS proved to significantly accelerate the procedure and led to more satisfied team members.

NCT ID: NCT00720681 Completed - Multiple Trauma Clinical Trials

Plating of Humeral Shaft Fractures in Multiple Trauma Patients.

HUMERUS
Start date: August 2008
Phase: N/A
Study type: Observational

The purpose of this study is to review our experience with the operative management of acute diaphyseal fractures of the humerus via an anterolateral approach with the use of small fragment fixation at a Level I, urban, trauma center. We will report our clinical and radiographic results, complication rate and final range of motion. A standardized outcome measurement (DASH) will be reported. Muscle recovery of the triceps and biceps will be evaluated by a standard protocol, accomplished with the assistance of a licensed physical therapist. We hypothesize that open reduction and internal fixation of humeral diaphyseal fractures via an antero-lateral approach with the use of small fragment fixation is a safe and efficacious way to treat multiple trauma patients with these injuries.