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Emergency Service, Hospital clinical trials

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NCT ID: NCT03955965 Completed - Clinical trials for Emergency Service, Hospital

Medication Reconciliation in an Emergency Department: How to Prioritize Patients ?

Start date: April 1, 2018
Phase:
Study type: Observational

Medication reconciliation has proven its efficiency in improving patients' care, especially for emergency patients. This study aimed to identify risk factors of unintended medication discrepancies (UMD) in an emergency department. Secondary objectives were to identify the number and type of UMD, correction rate of UMD and the impact of emergency department organisation on UMD.

NCT ID: NCT03818360 Completed - Smoking Cessation Clinical Trials

Deliver an Evidence-based Smoking Cessation Intervention for Smokers Attending A&E Departments in Hong Kong

Start date: August 13, 2019
Phase: N/A
Study type: Interventional

This project aims to deliver an evidence-based smoking cessation intervention comprising the provision of brief cessation advice to smokers attending emergency departments and active referral to existing smoking cessation services. The objectives are as follows: 1. To promote this evidence-based project to emergency departments in various hospitals under the Hospital Authority 2. To construct a network with non-governmental organisations (NGOs) to provide smoking cessation services 3. To train healthcare professionals to use the AWARD model to deliver brief cessation advice to smokers 4. To deliver brief cessation advice via healthcare professionals and actively refer smokers to existing smoking cessation services.

NCT ID: NCT03323229 Completed - Clinical trials for Emergency Service, Hospital

SatCare: Remote Support for Ambulance Clinicians in Medical Emergencies

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

SatCare is a randomised controlled trial involving rapid standardised ultrasound assessment of patients with shock, major trauma, abdominal pain, chest pain or breathlessness in emergency ambulances. The scans will take less than 5 minutes and be transmitted to a hospital-based expert for review, providing support and instructions for optimal prehospital care. Five Highland Scottish Ambulance Service ambulances covering areas more than 30 minutes from Raigmore Hospital, Inverness, UK, will be equipped with an ultrasound machine (M-Turbo, FujiFilm Sonosite) and satellite transmission system plus webcam, and will be deployed in real emergency situations. When dispatched to a potentially eligible patient, the attending paramedic will contact Raigmore Hospital's emergency department to check the availability of an emergency medicine specialist and obtain study group allocation (ultrasound with enhanced telecommunications plus usual care versus usual care alone). Following verbal consent from the patient, trained paramedics will perform the condition-specific scan protocol in the ambulance at the incident site, and transmit the recordings and patient video via satellite to the emergency department for specialist analysis. The consultant will give advice on patient management via standard ambulance communications systems while it is en route to the hospital. The remotely supported prehospital ultrasound implementation will be examined in terms of its delivery and functioning. An economic evaluation will compare its use with care as usual for eligible patients transported by ambulance, modelling the costs and benefits of this service expansion and determining optimum use. It is hoped that the results, anticipated to be available in 2019, will provide an evidence base for the use of prehospital ultrasound for emergency care.

NCT ID: NCT03309410 Completed - Clinical trials for Emergency Service, Hospital

Mathematical Arterialization of Venous Blood Gas

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

Objective: Arterial blood gas (ABG) analysis is essential in the clinical assessment of potential acutely ill patients. Venous to arterial conversion (v-TAC), a mathematical method, has recently been developed to convert peripheral venous blood gas (VBG) values to arterialized VBG (aVBG) values. The aim of this study was to test the reliability of aVBG compared to ABG in an emergency department (ED) setting. Method: Twenty ED patients were included in this study. ABG and three aVBG samples were collected from each patient. The aVBG samples were processed in three different ways for comparison: aVBG1 was held steady and analysed within 5 minutes; aVBG2 was tilted in 5 minutes and analysed within 7 minutes; aVBG3 was held steady and analysed after 15 minutes. All VBG samples were arterialized using the v-TAC method. ABG and aVBG samples were compared using Lin's Concordance Correlation Coefficient (CCC) and Bland-Altman's analysis.

NCT ID: NCT03208530 Completed - Clinical trials for Advance Care Planning

Motivational Interview Intervention to Help Patients Formulate Their Goals for Medical Care in the Emergency Department

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

Test the acceptability and feasibility of a brief motivational interview intervention to facilitate advance care planning (ACP) conversations for older adults with serious co-morbid illness being discharged from the emergency department (ED). The investigators will interview the participants to understand their perception of the intervention and collect patient-reported outcomes data after leaving the ED.

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: NCT02985177 Withdrawn - Acute Pain Clinical Trials

A RCT of a Combination of Analgesics for Pain Management in Children With a Suspected Fracture

CAST
Start date: January 2020
Phase: Phase 4
Study type: Interventional

MSK-I is the most common cause for ED visits for children with pain, with a child's risk of sustaining a fracture ranging from 27-42% by the age of 16 years. MSK-I is known to generate moderate to severe pain in most children and the ED serves as the critical entry point for these injured children. This study aims to provide rapid and sustained pain management for children presenting with a MSK-I in the ED. The investigators will compare the efficacy of two possible medication combinations of fentanyl intranasal (1.0 mcg/kg) + oral ibuprofen (10 mg/kg) and fentanyl intranasal (2.0 mcg/kg) + oral ibuprofen (10 mg/kg) for the rapid, adequate and sustained pain management of children with suspected fracture. The investigators believe that the combination of different dosage of intranasal fentanyl with ibuprofen will lead to better pain treatment by providing a consistent and adequate level of analgesia throughout the entire ED visit, including prior to physician exam and during painful radiologic procedures.

NCT ID: NCT02983409 Completed - Urinary Calculi Clinical Trials

Analysis the Relationship Between the Abdomen CT and Outcomes in Acute Urinary Stone Patients

Start date: January 2011
Phase: N/A
Study type: Observational

This is an observational study based on retrospectively collected data of ureter stone patients between 2011 and 2014. Aim of study is to determine radiologic findings of non-contrast abdominal computerized tomography as predicting clinical outcomes of suspect ureter stone patients in emergency department (ED).

NCT ID: NCT01815931 Completed - Emergencies Clinical Trials

Hemolysis in Blood Samples in the ER

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

In this study, we aim to identify risk factors for hemolysis in blood samples drawn in the ED.

NCT ID: NCT01540266 Completed - Communication Clinical Trials

Basel Discharge Communication Project

BACOP
Start date: July 2011
Phase: N/A
Study type: Interventional

Assessing whether structuring of discharge information improves the sender's recall capacity