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Emergencies clinical trials

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NCT ID: NCT03145467 Completed - Clinical trials for Acute Migraine Headache

Comparison of Oral Paracetamol and Zolmitriptan Efficacy in the Treatment of Acute Migraine in Emergency Department

Start date: January 2016
Phase: Phase 4
Study type: Interventional

Migraine is a chronic and sometimes progressive disorder, characterized by headache, recurrent episodes, and other associated symptoms. Migraine is the most common cause of headache among patients who applied to emergency services. The purpose of the investigators is to compare the efficacy of oral paracetamol and zolmitriptan in the treatment of acute migraine headache in an emergency department.

NCT ID: NCT03145454 Completed - Suffering, Physical Clinical Trials

Objective Markers of Pain Perception in Pediatric Emergency

TAMALOU
Start date: May 4, 2017
Phase: N/A
Study type: Interventional

Pain is a major problem in the care of children in pediatric emergencies. Indeed, its relief rests on the oral communication of the young patient, who does not always able to it (difficult to verbalize, fear of the hospital, problem mental development ...). There is no way in which pain can be apprehended objectively, immediately and effectively. To advance our knowledge of this problem, several approaches have been studied as from functional magnetic resonance imaging (fMRI), electroencephalography (EEG), or from autonomic parameters. However, all these approaches have their limitations: although fMRI presents interesting performances, it allows only a retrospective analysis, and cannot adapt to the clinical context of the young patient for example. EEG-based approaches and autonomic parameters show interesting results but suffer from perfectible sensitivity to muscle activation for EEG whereas the vegetative parameters to stress. In this context, our working hypothesis considers that the search for markers of painful perception must be based on a neurophysiological approach, based on the combined analysis of the EEG and autonomic responses in real time. The aim of this work is to study (1) the cortical (EEG) and autonomic (cardiovascular, skin, pupillary) responses induced by sutures in children who can communicate their pain according to whether they cause pain or not.

NCT ID: NCT03145389 Completed - Analgesia, Epidural Clinical Trials

Effect of Continuous Thoracic Epidural Analgesia on Gut Motility Following Emergency Laparotomy

Start date: March 20, 2016
Phase: N/A
Study type: Observational

Continuous thoracic epidural analgesia plays a very vital role in patients undergoing exploratory laparotomy. It not only supports a stable perioperative hemodynamics but also helps in early return of bowel activity.

NCT ID: NCT03143881 Completed - Heart Failure Clinical Trials

Assessment Of Educational Strategies In Heart Failure Patients Presenting To The Emergency Department For Care

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

This study evaluates the impact of a new education-based intervention on outcomes in un- and under-insured Heart Failure (HF) patients presenting to the Emergency Department (ED) for care. Intervention patients will receive personalized education regarding their condition, pre- and post-testing of their HF knowledge base, and ED standard of care during the enrollment (index) visit. Patients will then be contacted via telephone 30 days post-index visit for re-testing and reinforcement of previously learned material. Patients in the control group will receive ED standard of care.

NCT ID: NCT03139110 Completed - Mediation Clinical Trials

Impact of a Mediator for Patient Intake in Emergency Departments

MEDIA
Start date: November 15, 2017
Phase:
Study type: Observational

Violence in the workplace is becoming a serious phenomenon in the contemporary world of work. Hospital staff, like any employee working in contact with the public, is particularly exposed to this violence. In emergency departments, the number of patients treated and their heterogeneity, the problems of communicating with healthcare professionals, and waiting times, favor conflict situations. In the already tense context of the emergencies, the incivilities or violent acts have an impact on the well-being of professionals. In order to prevent these situations of violence, a solution could be to integrate a professional with specific skills into the teams to perform mediation functions between caregivers and patients. The aim of the study is to evaluate the impact of the presence of a mediator in emergency services on personal (verbal or physical) attacks on professionals (caregivers, doctors, administrative staff).

NCT ID: NCT03138707 Completed - Emergencies Clinical Trials

Patients Who Die Within Emergency Department

Start date: January 1, 2016
Phase:
Study type: Observational

Emergency services are a crowded and chaotic environment.

NCT ID: NCT03133767 Completed - Emergencies Clinical Trials

Saline vs. Lactated Ringers for Emergency Department IV Fluid Resuscitation

Start date: May 23, 2017
Phase: Phase 4
Study type: Interventional

Administration of intravascular (IV) fluid is the most common emergency department (ED) procedure. IV fluids are integral to increasing effective blood volume and ensuring organ perfusion in patients with volume depletion and dehydration. There are many options of IV fluids providers can use when treating ED patients. Surveys show physicians do not cite an evidence-based reason for selecting the crystalloid IV fluid used; the decision was likely to be influenced by type and location of practice. A gap exists in the current literature, as there is no evidence for the optimal IV fluid choice for the ED patient requiring IV fluid before discharge. Normal saline (NS) is commonly used as an IV fluid replacement in ED patients. However, NS has been associated with increased risk of acidosis and acute kidney injury. This study will use a novel approach of a patient-centered outcome in a non-critically ill population to ascertain the optimal IV fluid for patient quality of recovery. The results of this study will inform provider's IV fluid decisions between NS and LR. More importantly, the results of this study will have the power to improve patient's quality of recovery following IV fluid administration and subsequent ED discharge. ED patients will be recruited, and participants will be randomized to receive one of two IV solutions (Lactated ringer's or normal saline). Participants will answer a survey before and after the intervention to assess their quality of recovery. The post-survey will be administered by phone after ED discharge. Participants will also be contacted by text message one week following their ED visit to gather information on their healthcare utilization.

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: NCT03131609 Completed - Clinical trials for Urinary Tract Infections

Avoiding Bacterial Contamination of Clean Catch Urine Cultures in Ambulatory Patients in the Emergency Department

Start date: September 2015
Phase:
Study type: Observational

The purpose of this study is to find the best cleaning and collection methods to obtain a 'non-contaminated' clean catch mid-stream urine sample to diagnose suspected urinary tract infection (UTI).

NCT ID: NCT03127085 Completed - Atrial Fibrillation Clinical Trials

A.Fib Emergency Department Study Atrial Fibrillation

Start date: April 21, 2017
Phase:
Study type: Observational

Patients with a history of atrial fibrillation (AF) who frequently attend the emergency department (ED) with symptoms may not require emergency treatment, and may be more appropriately managed in an alternative outpatient setting. This may be the result of inappropriate or inadequate advice or a lack of patient understanding. The main research objective pertains to the reason for seeking medical attention for AF in the ED, ED management of the patient, outcomes of ED care and alternative strategies.