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Emergencies clinical trials

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NCT ID: NCT03254524 Completed - Diabetes Mellitus Clinical Trials

Geography of ED Use and Population Health

Start date: August 20, 2014
Phase:
Study type: Observational

The goal of this study is to create predictive models of emergency care and metrics for population health that can be used to analyze how events like hospital closures or disasters like Hurricane Sandy affect health care utilization by patients in specific populations or geographic regions. Additionally, it will allow the development of metrics for population health that can act as surveillance mechanisms to measure disease prevalence and identify patterns in emergency department use that can be used to identify specific geographic regions where health care is either optimized to promote health or needs to be improve so that population health can be improved.

NCT ID: NCT03250936 Completed - Trauma Clinical Trials

Descriptive Study of Trampoline Accidents in the Pediatric Emergency Department of Rennes

TRAUMPO
Start date: December 6, 2016
Phase: N/A
Study type: Observational

The aim of this study is to compare trauma related to others sport to trauma due to trampoline in pediatric emergencies of Rennes.

NCT ID: NCT03250884 Completed - Pregnancy Related Clinical Trials

Evaluation of the Performance of a Rapid Pregnancy Diagnostic Test.

Start date: August 30, 2016
Phase:
Study type: Observational

The aim of the study is to evaluate the effectiveness of a rapid pregnancy diagnostic test to improve the medical care of patients in emergency room.

NCT ID: NCT03246035 Completed - Heart Failure Clinical Trials

Reducing Readmission for Frail Elderly Patients With Decompensated Heart Failure

HFF-ED
Start date: March 1, 2018
Phase: N/A
Study type: Interventional

A randomized study designed to determine whether telephone based interventions can prevent return hospital visits for elderly and frail patients with acute symptoms of heart failure. Specifically, the intervention will improve patients ability to monitor and address self care of heart failure at home.

NCT ID: NCT03244436 Completed - Anesthesia Clinical Trials

Emergency Surgery Following Pediatric Catheterization

Start date: June 15, 2013
Phase: N/A
Study type: Observational

We study the outcome and prequesties of emergency surgeries that were necessary following accidents in the pediatric cardiac catheterization lab

NCT ID: NCT03239730 Completed - Respiratory Failure Clinical Trials

Arterial pH Selectively Predicts Intensive Care Unit Transfer From the Emergency Department in Obese Patients With Acute Dyspnea

Start date: May 23, 2013
Phase: N/A
Study type: Observational

This study evaluates the prognostic value of arterial blood gas analysis in a cohort of Emergency Department patients presenting with shortness of breath of any cause, comparing obese and non-obese patients.

NCT ID: NCT03229226 Completed - Emergencies Clinical Trials

Development and Assessment of a Simulation Model of Focused and Ongoing Professional Practice Evaluations

OPPE16
Start date: October 1, 2015
Phase: N/A
Study type: Observational

Since 2007, the Joint Commission on Accreditation of Healthcare Organizations (JCAHO) has required evaluation of practicing attending physicians by management to ensure that procedural skills and medical care are meeting the accepted standards of care as assessed by each individual institution. This assessment is known as the ongoing professional practice evaluation (OPPE). There are several methods by which this can be accomplished, including through chart review of clinician practice and by verbally assessing knowledge of the steps required to do a particular procedure. However, for infrequently performed or complicated procedures, these methods may not allow objective evaluation on a regular basis. Simulation using task trainers or manikin models offers an alternative method of objective evaluation in a standardized setting. The goal of this study is to develop two simulated scenarios to assess physician skill in relatively uncommon procedures and compare the data obtained against the verbal assessment and chart review model previously used at our institution. Two raters will assess each practitioner's verbal and simulated procedures. They will also assess globally their confidence that the physician is capable of performing the procedure safely and correctly based on the verbal or simulated trial. The investigators anticipate that using a simulated experience for assessment will increase the ability of raters to assess proficiency for the purposes of an OPPE, specifically by increasing the number of critical procedural components that can be objectively evaluated. The investigators hypothesize that there will not be a strong relationship between the scores obtained on the verbal assessment and the scores obtained on the task trainer assessment. The investigators anticipate that there will be a portion of study participants that do not meet a minimum passing standard and may require additional deliberate practice and further testing.

NCT ID: NCT03226366 Completed - Sepsis Clinical Trials

Effect of Emergency Department Care Reorganization on Door-to-antibiotic Times for Sepsis (LDS SWARM)

Start date: May 16, 2015
Phase:
Study type: Observational

Sepsis is a common syndrome resulting from a dysregulated response to infection. The timing of antibiotic initiation is an important determinant of outcomes for patients presenting to the emergency department with sepsis. The potential effect of care reorganization on very early care for sepsis is unknown. This study will investigate whether multidisciplinary coordination of the initial patient evaluation in the emergency department influences door-to-antibiotic time for septic patients.

NCT ID: NCT03216941 Completed - Clinical trials for Psychiatric Disorder

Randomised Trial Ketiapine Olanzapine Fast Sedation Agitated Patients Emergency Ward

IM-OK-FAST
Start date: January 1, 2015
Phase: Phase 4
Study type: Interventional

comparison of intramuscular olanzapine and ketamine efficacy as first medication for fast sedation of patients with agitation and aggressive behavior. Five hundred patients with agitation caused by psychiatric disorder were randomly assigned under double-blind conditions to receive olanzapine or ketiapine. The Overt Agitation Severity Scale, Overt Aggression Scale and Ramsay Sedation Scale will be applied within 12 hours after the first dosage.

NCT ID: NCT03213197 Completed - Patient Education Clinical Trials

Feasibility of a Standardized Video for Patient Education and as a Decision Aid on Code Status for Patients in the Emergency Department Pending Admission to the Hospital

Start date: February 14, 2017
Phase: N/A
Study type: Interventional

The researchers hypothesize that patients and their families will be comfortable watching standardized CPR informational videos and that they would recommend that others watch the videos. Furthermore, the researchers hypothesize that patients and their families will find the videos helpful in their own end-of-life planning.