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Trauma clinical trials

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NCT ID: NCT03070834 Completed - Pulmonary Embolism Clinical Trials

RIPT Feasibility Trial

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

The risk of venous thromboembolism (VTE) is very high in trauma patients, secondary to tissue injury, venous status from immobilization, and thrombophilia. As such, early initiation of VTE prophylaxis is essential in this population. The competing risks of life threatening hemorrhage and VTE need to be considered very carefully. Potential approaches to VTE prophylaxis include pharmacologic means, and mechanical devices. For patients unable to receive pharmacologic VTE prophylaxis, retrievable inferior vena cava filters (rIVCFs) may be placed until low molecular weight heparin (LMWH) can be initiated, as per guidelines such as Eastern Association for the Surgery of Trauma The investigators propose a feasibility study to determine whether or not our center can insert rIVCFs in at-risk trauma patients expeditiously enough to cause a meaningful reduction in the time they are left unprotected to PE.

NCT ID: NCT03069755 Completed - Trauma Clinical Trials

Perioperative Mortality Rate in Indian Trauma Patients

Start date: January 2017
Phase:
Study type: Observational

This study aims to estimate the perioperative mortality rate in adult trauma patients undergoing acute surgery as well as the association between type of acute surgery and perioperative mortality in university hospitals in urban India.

NCT ID: NCT03068104 Completed - Trauma Clinical Trials

Unmet Need for Massive Transfusion in Indian Trauma Patients

Start date: January 2017
Phase:
Study type: Observational

This study aims to estimate the difference between predicted and provided massive transfusion in adult trauma patients admitted to university hospitals in urban India.

NCT ID: NCT03023839 Completed - Delirium Clinical Trials

Incidence and Risk Factors for Delirium in Severely Injured Patients

Start date: February 2015
Phase: N/A
Study type: Observational

Delirium is very common in intensive care unit (ICU) patients and leads to poor outcomes. There is little information on delirium in injured patients however. This study determined the incidence and risk factors for delirium in severely injured patients.

NCT ID: NCT02999386 Completed - Diabetes Mellitus Clinical Trials

Stress Induced Hyperglycemia In Trauma

SIHG
Start date: October 2016
Phase:
Study type: Observational

The clinical relevance of the observed stress induced hyperglycemia in trauma patients remains unclear. The earlier studies suggested the implications of cytokines in stress induced hyperglycemia and the outcomes after trauma. To date, there is little information available regarding the effect of diabetic hyperglycemia (occult or known) on outcomes after trauma and whether these patients represent a distinct group with differential outcomes when compared to those with stress-induced hyperglycemia. Herein, the purpose of this study is to identify the incidence of stress induced hyperglycemia as well as diabetic hyperglycemia in trauma patients and to investigate the association between proinflammatory cytokine levels and hyperglycemia in our trauma population.

NCT ID: NCT02984384 Completed - Trauma Clinical Trials

PREVENTion of Clot in Orthopaedic Trauma

PREVENT CLOT
Start date: April 24, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare aspirin versus low-molecular weight heparin (LMWH) (Enoxaparin) as a thromboprophylaxis in patients who sustain a fracture.

NCT ID: NCT02877875 Completed - Depression Clinical Trials

Student Outcomes of Integrative Mental Health Services

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

The study will compare the impact of Child STEPs (see Weisz et al., 2012) versus usual school-based therapy on students' mental health and school-related outcomes, and test whether changes in school outcomes are mediated by changes in student mental health.

NCT ID: NCT02864875 Completed - Trauma Clinical Trials

Early Administration of Fibrinogen in Polytraumatized Patients With Hypofibrinogenemia: a Randomized Feasibility Trial

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

This is a randomized feasibility trial conducted with severe trauma patients. At admission patients presented hypofibrinogenemia, hypotension and tachycardia. The primary outcome was feasibility assessed by the proportion of patients receiving the allocated treatment up to 60 minutes after randomization. The treatments regards to receive or not to receive an early replacement of fibrinogen.

NCT ID: NCT02856789 Completed - Trauma Clinical Trials

Determination of Fibrin Activity in Plasma on STA-R® Prototype

FAST
Start date: August 2016
Phase:
Study type: Observational

The purpose of the study is to give the proof of concept of the Fibrin structure assay on STA-R® prototype. It aims to identify the parameters which discriminate the pathologic from the normal population. Secondary objectives are to determine the precision of the assay, to record the Fibrin activity, comparatively with thromboelastography on TEG®, in a coagulation activation assay and in a coagulation-lysis assay.

NCT ID: NCT02838459 Completed - Trauma Clinical Trials

Can Prediction Models Triage Trauma Patients More Accurately Than Clinicians?

Start date: July 2016
Phase:
Study type: Observational

Using a prospective cohort design, the aim of this study is to compare the performance of clinicians with prediction models in triaging trauma patients.