Clinical Trials Logo

Major Trauma clinical trials

View clinical trials related to Major Trauma.

Filter by:

NCT ID: NCT04144803 Active, not recruiting - Anesthesia Clinical Trials

Brain Oxygenation During Prehospital Anesthesia: an Observational Study

BOPRA
Start date: November 18, 2019
Phase:
Study type: Observational

Brain oxygenation of adult patients undergoing prehospital emergency anesthesia is monitored using noninvasive near-infrared spectroscopy. Patients are afterwards interviewed to define neurological outcome to measure quality of life. The purpose of this study is to reveal the risk factors of prehospital anesthesia related cerebral desaturation events (CDE) and to define the association between CDE and survival, neurological outcome or quality of life.

NCT ID: NCT03986736 Completed - Major Trauma Clinical Trials

Markers of Tissue Injury and Rhabdomyolysis in Patients With Major Trauma

Start date: June 15, 2019
Phase:
Study type: Observational

Major trauma is associated with a release of alarmins (DAMPs - damage-associated molecular patterns) from the injured tissues. This process results in the activation of the immune system, which is one of the main mechanisms participating in the development of organ dysfunctions in patients with major trauma.

NCT ID: NCT03736005 Completed - Quality of Life Clinical Trials

Skeletal Muscle Wasting and Renal Dysfunction After Critical Illness Trauma - Outcomes Study

KRATOS
Start date: December 19, 2018
Phase:
Study type: Observational

This study aims to determine changes in kidney function during and after critical illness, comparing conventional creatinine based methods with the gold standard to accurately establish the presence of new or worsened chronic kidney disease. In addition, investigators will assess the confounding effect of muscle wasting on the conventional assessment of kidney function and investigate the information that measures of kidney function may contribute to the assessment of musculoskeletal health after critical illness.

NCT ID: NCT03354559 Completed - Major Trauma Clinical Trials

Trauma Associated Bleeding: Effectiveness of an Early Coagulation Support Protocol

Start date: January 1, 2011
Phase: N/A
Study type: Observational

In severe trauma patients, uncontrolled bleeding is a major cause of death, partly caused by trauma-induced coagulopathy (TIC).TIC represents a severe post-traumatic complication associated with increased transfusion requirements and worsened mortality. Fibrinolysis is a central part of the TIC process. Massive Transfusion Protocols (MTPs) were introduced as part of damage control resuscitation, with the aim to facilitate rapid blood product release and to increase adherence to hemostatic resuscitation, In 2013, the Italian Trauma Centers Network (TUN) developed a new treatment algorithm providing early coagulation support (ECS) to control coagulopathy and hemorrhage in major trauma patients with a clinically relevant bleeding risk. The protocol includes the use of fibrinogen concentrate and RBC during initial resuscitation, and the early use of viscoelastic techniques when available (thromboelastometry ROTEM® or thromboelastography TEG). The aim of this multicenter, before and after study was to assess the effects of a new ECS protocol compared to the standard MTP in terms of blood products' consumption and clinical outcome.

NCT ID: NCT03259776 Completed - Major Trauma Clinical Trials

Experiences of Visitors to a Regional Major Trauma Intensive Care Unit

VISIT_ICU
Start date: November 16, 2017
Phase:
Study type: Observational

Since 2011, people who have had a serious accident in England are no longer looked after at the hospital nearest to them. Instead, they are cared for at a specialist hospital called the regional major trauma centre. This is so that they can get the best possible care from specialist professionals. St George's is the regional major trauma centre for the 2.6 million people living in South West London and Surrey County. This area stretches about 40 miles across. About one fifth of major trauma patients who come to St George's live more than one hour's journey away. Their visitors often travel a similar distance or even further. Family members and friends play an important part during the patient's stay. It is important to support visitors. The aim of this study is to describe the experiences of visitors whose family member or friend has been admitted to the major trauma intensive care unit at St George's. In particular, the aim is to describe the experiences of visitors who travel from far. First, ten visitors will be interviewed to find out more about their experiences. From these data, a survey questionnaire will then be developed and approximately 150 visitors who have been to St George's in recent months will be surveyed. This will give in-depth insights to understanding peoples' experiences of visiting at St George's, and what people thought was going well and things that could be better. The study will end with a service improvement workshop with representatives from the team at St George's and visitors. Study findings will be discussed and decisions on what should be improved will be made. This study is being funded by St George's Hospital Charity. The study runs from August 2017 to October 2018.

NCT ID: NCT03005509 Completed - Major Trauma Clinical Trials

Structured Trauma Quality Improvement Meetings at Four Trauma Centres in India

TQI
Start date: January 2017
Phase: N/A
Study type: Interventional

A prospective before-and-after study to evaluate the effect of implementing a Trauma Quality Improvement protocol on the process of Trauma Quality Improvement meetings and major trauma patient outcomes at four trauma centres in India.

NCT ID: NCT02877342 Recruiting - Major Trauma Clinical Trials

Pre-hospital Notification of Injured Patients Presenting to Trauma Centres in India

Start date: March 2016
Phase: N/A
Study type: Observational

A prospective observational study using an interrupted time-series design to evaluate the effect of pre-hospital notification on trauma patients arriving at a trauma centre by ambulance, in India

NCT ID: NCT02509390 Recruiting - Major Trauma Clinical Trials

Hyperfibrinogenemia After Major Trauma

Start date: September 2014
Phase: N/A
Study type: Interventional

Assessment of the evolution of fibrinogen plasma level within the first ten days after major trauma in order to determine prevalence of hyperfibrinogenemia (Fg > 4 g/L) and its time to onset.

NCT ID: NCT02165137 Completed - Trauma Clinical Trials

Management of Major Trauma Patients at Aarau Trauma Center - Evaluation of Processes and Patient Outcome

Start date: January 2010
Phase:
Study type: Observational [Patient Registry]

Quality control and improvement project: Assessment and analysis of processes and outcome in trauma emergency room and major trauma patients at the Aarau trauma center (cantonal hospital) with regard to initial emergency management, hospital processes and short- and long-term (1-and 2-year) outcome of patients (subjective and objective). Comparison of processes and outcome pre- and post- project initiative. Benchmarking with the literature and by participation in the German and Swiss Trauma registry each.

NCT ID: NCT02000674 Completed - Shock Clinical Trials

Succinylcholine vs Rocuronium for Prehospital Emergency Intubation

CURASMUR
Start date: December 2013
Phase: Phase 3
Study type: Interventional

All adult patients with spontaneous cardiac activity and requiring tracheal intubation in the pre hospital emergency context will be included in order to compare the use of succinylcholine vs Rocuronium for prehospital emergency intubation.