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Trauma clinical trials

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NCT ID: NCT03191279 Not yet recruiting - Trauma Clinical Trials

First Aid by Laypersons - Effect on Mortality and Length of Stay

Start date: August 2018
Phase: N/A
Study type: Observational

The study aims to assess the effect of first aid from bystanders on survival, admission length, and need of ICU-stay for trauma victims.

NCT ID: NCT03170401 Completed - Critical Illness Clinical Trials

Supplemental Enteral Protein in Critical Illness

Start date: November 2016
Phase: Phase 3
Study type: Interventional

The aim of this study is too determine the effect of enteral protein supplementation on biochemical measures of inflammation and protein metabolism in critically ill surgical patients. The investigators will also collect data on important clinical outcomes, including infectious complications, duration of mechanical ventilation and other measures of recovery from critical illness. Hypothesis: That early supplemental protein will increase serum concentrations of transthyretin at three weeks after the onset of illness or injury. Secondarily, the investigators will test whether supplementation, reduces infectious complications and increases ventilator-free days.

NCT ID: NCT03162679 Completed - Trauma Clinical Trials

Culture-sensitive Emotion Regulation Group Therapy for Traumatized Refugees

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

There is a lack of studies on treatment effect in traumatised refugees. Recent findings indicate that emotion regulation deficits play a key role in PTSD also among traumatized refugees and highlight the importance and potential directions for the development of an emotion regulation training for refugees. In this study, the investigators therefore want to examine the effectiveness of a new, transdiagnostic, cultural-sensitive group therapy, which systematically teaches specific emotion regulation strategies. Participants will be randomly assigned to either the emotion regulation training, delivered in group format or a wait list control condition. The study takes place in cooperation with REFUGIO Munich, which is a treatment centre specialised in the treatment of traumatised refugees. Clinicians will deliver the treatment to traumatized asylum seekers and refugees that report difficulties in emotion regulation. The investigators will examine if refugees and asylum seekers in the intervention group will show improvements in psychological symptoms, social functioning as well as in emotion regulation in comparison to a wait list control group which will receive the treatment after the intervention group has completed. The group therapy covers 14 sessions and has a cognitive-behavioural background. It focuses on conveying strategies to cope with intense feelings and the patients should gain a sense of self-efficacy and control over their trauma-relevant feelings and symptoms. Qualified interpreters will be used in the assessments as well as group therapies.

NCT ID: NCT03159078 Recruiting - Critical Illness Clinical Trials

Polymyxin B Monotherapy vs Combination Therapy in Critically Ill Patients With Multi-drug Resistant Pathogens

MUSEUM
Start date: May 25, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of polymyxin B as monotherapy versus a combined polymyxin B-carbapenem therapy against multidrug-resistant (MDR) gram negative infections. The investigators intend to evaluate if this synergistic drug regimen correlates with improved outcomes against gram-negative infections in critically ill patients including: better clinical resolution, reduced length of stay at hospital, reduced length of stay at the intensive care unit, and less recurrence of infection.

NCT ID: NCT03155490 Completed - Trauma Clinical Trials

Study of Team Leadership Training Effect on Patient Care

Start date: April 2016
Phase: N/A
Study type: Interventional

Brief Summary: Trauma is a major public health burden; it is the fifth most common cause of mortality overall in the US and accounts for the majority of deaths in patients younger than 45. Trauma resuscitations present unique patient care challenges due to the need to perform complex tasks under uncertain and time-pressured conditions. It is not entirely surprising that one-third to one-half of trauma patient-related errors occurred in emergency departments during the initial resuscitation period. Effective team leadership can enhance teamwork and team adaptability, thus improving teams' ability to handle unexpected and rapidly changing situations. Simulation-based training provides a clinically relevant practice environment that has been recommended for team and team leader training. The purpose of this research is to evaluate the impact of simulation-based leadership training on clinical teamwork, team leadership and patient care. The investigators hypothesize that team leadership training will improve team leadership, teamwork, and critical patient care events during actual trauma resuscitations.

NCT ID: NCT03153904 Completed - Depression Clinical Trials

Connecticut Child STEPs

Start date: October 2013
Phase: N/A
Study type: Interventional

Connecticut Child STEPS is a randomized controlled trail investigating the effectiveness of MATCH-ADTC in treating anxiety, depression, trauma, and/or behavioral problems in children seeking services at four Department of Children and Families (DCF) funded clinics in the state of Connecticut. The study will evaluate child outcomes following two forms of therapist training in the MATCH model.

NCT ID: NCT03141502 Not yet recruiting - Trauma Clinical Trials

The New Skin Stretching Device for Treatment of Limb Tension Wounds

SSDRCT
Start date: May 11, 2017
Phase: Phase 4
Study type: Interventional

A randomized controlled trial is performed to evaluate the effectiveness and safety of the Skin Stretching Device (SSD) on limb tension incision closure by comparing whether the differences in wounds area, wounds closure time and scar assessment between the SSD and the skin grafting are statistically significant.

NCT ID: NCT03133702 Completed - Trauma Clinical Trials

Traumatic Characteristics of the Forensic Cases Admitted to Emergency Department and Errors in the Forensic Reports

Start date: January 1, 2014
Phase: N/A
Study type: Observational

Objectives: to detect the mistakes and deficiencies of the forensic reports which was written and to detect the injury characteristics of the forensic cases applied to emergency service of a tertiary hospital.

NCT ID: NCT03128658 Completed - Trauma Clinical Trials

Trauma Induced Coagulopathy and Inflammation

TrICI
Start date: February 27, 2017
Phase:
Study type: Observational

While a number of factors are known to be associated with the development of trauma induced coagulopathy (TIC), inflammation, and multi-organ failure, we currently cannot predict which patients are at risk for developing these life threatening conditions with any certainty. In this prospective observational study, we will investigate the many factors that contribute to the development of trauma induced coagulopathy, post injury inflammation and the development of organ dysfunction in order to develop a multi scale computational algorithm of clinical prediction. Using a convenience sample technique, demographic data, physiologic data, blood samples and clinical variables will be collected over 5 days following traumatic injury. A computational model will be used to predict the development of TIC and multi-organ failure.

NCT ID: NCT03123328 Completed - Trauma Clinical Trials

Evaluation of Non-Invasive Hemoglobin in Trauma Patients

Start date: June 30, 2016
Phase: N/A
Study type: Interventional

This is a prospective, non-blinded, non-randomized, interventional study of the Masimo pulse oximeter and sensors in a trauma setting