Clinical Trials Logo

Emergencies clinical trials

View clinical trials related to Emergencies.

Filter by:

NCT ID: NCT03052192 Active, not recruiting - Aging Clinical Trials

Biological Aging, Medication, Malnutrition and Inflammation Among Acutely Ill and Healthy Elderly.

FAM-CPH
Start date: November 2016
Phase:
Study type: Observational

In this study, the investigators will investigate and characterize acute medical patients in order to optimize patient courses in the acute care departments, especially with regard to polypharmacy and undernourishment. In addition, the investigators will investigate underlying immunological mechanisms of chronic inflammation and biological aging in this population to improve the current knowledge and possibilities for preventing chronic diseases and acute hospitalization.

NCT ID: NCT03017248 Active, not recruiting - Pain Clinical Trials

Low-dose Ketamine for Acute Pain in the Emergency Department

Start date: January 2016
Phase: Phase 1
Study type: Interventional

This study aims to determine the efficacy and safety of low dose ketamine in association with IV morphine in the management of acute moderate to severe pain in emergency department. The investigators hypothesize that low dose ketamine will result in more effective pain control than morphine alone and will not be associated with an increase in adverse events.

NCT ID: NCT02887300 Active, not recruiting - Clinical trials for Psychological Stress

Mantra Meditation to Reduce Emotional Exhaustion in Emergency Department Staff

Start date: January 31, 2017
Phase: N/A
Study type: Interventional

Work in a healthcare setting, such as in an emergency department (ED), while rewarding, can be harmful to psychological well being, as demonstrated by the high numbers of Irish hospital doctors experiencing burnout. Burnout has been linked to poor healthcare quality, medical errors and low patient satisfaction. To prevent further escalation of this problem, there is a need for effective stress-reducing intervention, such as meditation. Meditation practice has a confirmed positive effect on well being; through greater insight and awareness, meditation could help ED staff to become more attentive to and understanding of their patients' complaints, enhancing patient satisfaction and safety. However, based on current research it is difficult to distinguish between the effects of meditation on well being and those associated with bringing people together. There is therefore a need for a larger randomised study (RCT) including a participants that receive no meditation intervention. This pilot study aims to examine the suitability of RCT to assess the effect of mantra meditation on burnout among ED staff. The investigators will also examine participant recruitment and retention, data management and outcomes assessment methods for well being, patient satisfaction and biological markers. There will be two groups: intervention group (meditation) and control group (non-meditation). 30 ED staff placed in the intervention group will discuss prescribed texts and learn mantra meditation over a 7-week period, accompanied by 20 minutes of daily meditation practice. 30 ED staff placed in the control group will work in the ED as usual and not receive any texts. Biological samples and questionnaires will be obtained at three time points. Participant feedback will also be sought through interviews. This study will highlight issues related to participant recruitment, retention, and adherence, questionnaires, logistics, and data management and pave the way for an efficient, effective, and larger study that will investigate mantra meditation as a means of reducing burnout in ED staff.

NCT ID: NCT02887066 Active, not recruiting - Clinical trials for Acute Coronary Syndrome

Observatory on Emergency Care for Acute Coronary Syndrome in Grand Est of France

CHEST
Start date: September 2014
Phase: N/A
Study type: Observational

The purpose is to build up a data observatory of individuals with thoracic pain evoking acute coronary syndrome (ACS). The aim is the characterization of this population of patients consulting at emergency department, the evaluation of therapeutic strategies with regard to guidelines and the becoming of patients including severe complications and mortality.

NCT ID: NCT02866266 Active, not recruiting - Clinical trials for Opioid-related Disorders

ER/LA Opioid Surveillance for Emergency Department Visits and Hospitalizations for Overdose and Poisoning

Start date: n/a
Phase: N/A
Study type: Observational

Study to evaluate the impact of the ER/LA opioid REMS program on the incidence of Emergency Department visits and hospitalizations for overdose/poisoning and death among patients prescribed ER/LA opioid analgesics.

NCT ID: NCT02754245 Active, not recruiting - Clinical trials for Emergency Department Overcrowding

ED Overcrowding Validation Study

EDOVS
Start date: November 14, 2016
Phase: N/A
Study type: Observational

The aim of this study is to externally validate a new emergency department overcrowding estimation tool (SONET) developed at John Peter Smith Health Network (JPS).

NCT ID: NCT02581267 Active, not recruiting - Clinical trials for Emergency Services, Psychiatric

Missed Serious Medical Illness in Psychiatric Patients Seen in an Academic Emergency Department

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

Psychiatric presentations are common in the emergency department (ED), and determining whether or not a psychiatric presentation is due to medical illness can be a difficult task for the emergency physician. The investigators define "serious medical illness" (SMI) as a pathological condition that would necessitate inpatient treatment on a medical or surgical ward. It is important for patient safety that SMI be triaged by the emergency physician to the appropriate inpatient service. The rate of missed SMI in patients with psychiatric presentations to the ED is unknown. The investigators will research missed SMI in patients referred to adult psychiatry from the ED, with the intent to improve patient safety.

NCT ID: NCT02466620 Active, not recruiting - Body Weight Clinical Trials

A Comparison of Paediatric Weight Estimation Methods for Emergency Resuscitation

Start date: February 2015
Phase: N/A
Study type: Observational

The purpose of this study is to study the validity, reliability and practicality of the different weight estimation methods (parent estimation method, Mercy method, Broselow tape, original and update APLS) in Thai children.

NCT ID: NCT02387112 Active, not recruiting - Clinical trials for End Stage Heart Disease

Early Versus Emergency Left Ventricular Assist Device Implantation in Patients Awaiting Cardiac Transplantation

Start date: July 2015
Phase: N/A
Study type: Interventional

The aim of the study is to assess whether, in patients who are listed for cardiac transplantation in transplantable (T) status, early implantation of a left ventricular assist device is superior to the current therapeutic strategy of medical heart failure therapy and assist device implantation only after serious deterioration of the patient's condition.

NCT ID: NCT02336217 Active, not recruiting - Diabetes Mellitus Clinical Trials

Glycemic Emergency Management (GEM); An App for Rapid Response to Hypoglycemic and Hyperglycemic Situations

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

The purpose of this pilot study is to determine the utility of an algorithm for better glucose control in diabetic patients communicated via an App to help improve outcomes and reduce urgent care and ER visits as well as improve A1C and quality of life.