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Emergencies clinical trials

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NCT ID: NCT02858531 Completed - Elderly Clinical Trials

Predictive Tracking of Patient Flow in the Emergency Services During the Virus Winter Epidemics

PREDAFLU
Start date: September 1, 2016
Phase:
Study type: Observational

Epidemics and infectious diseases in general, punctuate much of the activity of an emergency service. The impact of winter infections is particularly important to vulnerable populations such as infant during bronchiolitis epidemics and the elderly during seasonal influenza. Each year, these epidemic phenomena lead to disorganization of emergency services and healthcare teams by lack of anticipation and organizational measures in particular to manage the approval of emergency services for the most vulnerable populations requiring hospitalization. For 2 years, the pediatric emergency department of St Etienne University Hospital has a decision support tool for the periods of winter epidemics. Through a retrospective analysis of Passages of Emergency summary, this tool provides an estimate of infants with bronchiolitis flow day to day, and the availability in real time of an abnormally high flow of patients to pediatric emergencies. These data can help to affirm that the epidemic begins in this hospital.

NCT ID: NCT02854020 Completed - Emergency Clinical Trials

Comparison of Inflight First Aid Performed by Cabin Crew Members and Medical Volunteers

Start date: July 2014
Phase: N/A
Study type: Observational

Since the number of air travelers, including the elderly and passengers with an underlying disease, is increasing every year, the number of inflight emergency patients is expected to increase as well. The investigators attempted to identify the incidence and types of inflight medical emergencies and analyze the first aid performed by cabin crew members or medical volunteers in flights by an Asian airline. The investigators also investigated the causes of inflight deaths and aircraft diversions.

NCT ID: NCT02851771 Completed - Pneumonia Clinical Trials

Improving the Diagnosis of Pneumonia in Emergency Rooms

Start date: June 14, 2013
Phase: N/A
Study type: Interventional

A point-of-care laboratory (POC) was set at North Hospital, Marseille, France for the diagnosis in less than two hours of pneumonia caused by known pathogens, close to the reception of Emergency service. In this instance 30% of patients have no etiological diagnosis after the POC tests Pneumonia. This lab has discovered over 200 new species of bacteria in humans, including vector bacteria and opened the field of large Deoxyribo Nucleic Acid (DNA ) viruses. Also, the laboratory of emerging viruses discovered many Ribo Nucleic Acid (RNA) viruses transmitted by arthropods. Based on this collection of new pathogens described in POC laboratory, this study proposes to expand the etiological diagnosis strategy of pneumonia after POC tests.

NCT ID: NCT02841254 Completed - Meningitis Clinical Trials

Diagnostic Performance of Clinical Signs Patients Suspected of Meningitis to Emergencies

MEDWATCH
Start date: November 2014
Phase: N/A
Study type: Observational

Meningitis are serious infections. Evidenced by high rates of mortality and sequelae. However, these diseases have a relatively small impact. Also physician services Home Emergencies they must be vigilant, alert, for clinical signs to be suspected meningitis. Indeed, it is only after this essential clinical milestone that will be carried out a lumbar puncture which will confirm the diagnosis and to quickly begin treatment. Unfortunately, if recent studies can improve the therapeutic management of patients with meningitis, no study was interested in yet fundamental step of diagnosis. It seems therefore necessary to achieve a prospective clinical study to reassess the adequacy of the clinical signs in the diagnosis of meningitis. The ideal would be to achieve a predictive clinical score of the presence or absence of meningitis.

NCT ID: NCT02836665 Completed - Clinical trials for Dermatological Emergency

Application of Telemedicine for Dermatological Emergency Patients

Telederm
Start date: August 2016
Phase: N/A
Study type: Interventional

After admission to the emergency room each dermatological patient is routinely assessed to Manchester Triage System (MTS) by the nursing staff. Thereby data are collected for anamnesis followed by randomization in two equal study groups. Patients of group A (control group) wait routinely until the dermatological investigator in charge arrives at the emergency room. Once the dermatological investigator is on site, he gives a diagnosis and proposes a therapy. For Patients of group B (teledermatology) study-related photographs of the skin lesion and anamnesis data are uploaded to the hospital information system "medico". Those data can directly be processed by the dermatological investigator in charge who enters his diagnosis and his therapy proposal. Subsequently an internal control is carried out as the same investigator comes personally to the emergency room to check its telemedical diagnosis and therapy proposal. Finally both time periods patients have to wait in the emergency room for their diagnosis and therapy are compared with each other.

NCT ID: NCT02835963 Completed - Heart Failure Clinical Trials

Acute Heart Failure Study in Patients Admitted to Emergency Department for Dyspnea

PREDICA
Start date: March 2016
Phase:
Study type: Observational

No studies have analyzed the predictive value of different anamnestic and clinical signs for the diagnosis of acute heart failure (AHF) in patients admitted to emergency department. That's why the expert group of the AHF of South West of France mobilizes to conduct this study to evaluate the diagnostic predictive value of different anamnestic and clinical signs for the diagnosis of AHF to emergencies.

NCT ID: NCT02835053 Completed - Geriatrics Clinical Trials

Frailty and Postoperative Outcomes After Emergency General Surgery

Start date: April 2002
Phase: N/A
Study type: Observational

The investigators will examine the association between preoperative frailty and postoperative outcomes and resource utilization after emergency general surgery.

NCT ID: NCT02825082 Completed - Surgery Clinical Trials

Emergency Surgery in the Elderly: Comparison of Frailty Index and Surgical Risk Score

FRAILESEL
Start date: January 2017
Phase:
Study type: Observational

EMERGENCY GENERAL SURGERY IN GERIATRIC PATIENTS: EPIDEMIOLOGY, AND EVALUATION OF FACTORS AFFECTING MORBIDITY AND MORTALITY

NCT ID: NCT02823704 Completed - Fatal Outcome Clinical Trials

Proadrenomedullin for Early Risk Assessment in the Emergency Department

ADRISK
Start date: June 2016
Phase: N/A
Study type: Observational

The study ia aiming to the assessment of Mid-Regional proadrenomedullin (MR-proADM) as a novel biomarker that can provide accurate short-, mid- and long term prognostic information in the triage and multi-dimensional risk assessment of patients in the Emergency Department (ED). A clinical algorithm with predefined MR-proADM cut-off values: <0.75 nmol/L (low risk), 0.75 nmol/L≥ and ≤ 1.5 nmol/L (intermediate risk); >1.5 nmol/L is pre-defined. Based on these cut-off values, a prespecified algorithm aiming to predict i) reduction of hospitalization in the ward/ICU and increase of out-patient treatment (rule-out of risk); and ii) reduce adverse complications (identify patients at risk) will be applied and compared with the initial clinical decision.

NCT ID: NCT02821065 Completed - Heart Failure Clinical Trials

Telehealth for Emergency-Community Continuity of Care Connectivity Via Home-Telemonitoring

TEC4Home
Start date: October 31, 2016
Phase: N/A
Study type: Interventional

Modern technology like computers, smartphones and the Internet enable patients to measure certain health indicators, like blood pressure and body weight, from the comfort of their own homes. This information can also be shared electronically with doctors and other healthcare providers to monitor remotely. This is called home health monitoring. In TEC4Home, we are developing a home monitoring solution for patients with heart failure to support their care and recovery at home after a visit to the emergency department. We hope to show that this solution decreases revisits to the emergency department and increases quality of life for patients.