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Emergency clinical trials

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NCT ID: NCT02617875 Completed - Emergency Clinical Trials

Telemedical Support for Prehospital Emergency Medical Service

TEMS
Start date: July 9, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and quality of a pre-hospital holistic multifunctional teleconsultation system. This system consists of on-line transmissions of vital parameters, audio- and video-signals from the scene to a telemedicine centre, where a trained emergency physician (tele-EMS physician) uses software-based guideline conform algorithms for diagnosis and treatment. At the prehospital emergency scene half of the patients will receive this telemedicine-based approach and the other half the conventional emergency physician-based care.

NCT ID: NCT02610205 Completed - Emergency Clinical Trials

Caring Touch as a Bodily Anchor for Patients After Sustaining a Motor Vehicle Accident

Start date: September 2012
Phase: N/A
Study type: Observational

The aim of this study was to explore participants´ subjective experiences and perspectives on pain and other factors of importance after an early nursing intervention consisting of "caring touch" (tactile massage and healing touch) for participants subjected to a motor vehicle accident with minor or no physical injuries.

NCT ID: NCT02377687 Completed - Surgery Clinical Trials

Is Life Worth Living After Major Emergency GI Surgery? Patient Reported Outcome in Elderly Emergency Surgery Patients

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

To study the impact of emergency high risk GI surgery on HRQOL in elderly patients, seventy-five years or above and to explore the patients' experience with the informed consent process and the status 6 months after surgery.

NCT ID: NCT02297113 Completed - Emergency Clinical Trials

Rapid Sequence Intubation at the Emergency Department

Start date: November 2014
Phase: N/A
Study type: Interventional

All patients undergoing emergent endotracheal intubation (RSI) at the Emergency Department will be screened for inclusion in this clinical study. The indication of endotracheal intubation is an exclusively clinical decision and is not affected by this study protocol in any aspect. If fulfilling the In- and exclusion criteria's, patient will be randomly assigned to one of two groups 1. C-MAC Videolaryngoscope in appropriate size 2. conventional endotracheal intubation using Macintosh Blade in appropriate size Randomization (1:1) will be based on computer-generated codes maintained in sequentially numbered opaque envelopes that will be opened immediately before randomization.

NCT ID: NCT02040896 Completed - Emergency Clinical Trials

Who Contributes to the Ordering of CT Scans in Emergency Department Patients?

Start date: January 2014
Phase:
Study type: Observational

The primary objectives are: 1. To investigate which healthcare workers and other individuals contribute to the decision to order computed tomography (CT) scans for emergency department (ED) patients. 2. To investigate the specific reasons healthcare workers and other individuals order or request CT scans for ED patients. 3. To determine the frequency of clinically important actions following CT scan results. Once the drivers of ED CT utilization are identified, interventions including education, incentives for compliance with evidence-based best practices, and interventions for noncompliance could be targeted appropriately.

NCT ID: NCT01984645 Completed - Emergency Clinical Trials

Primary-care-provider Identification And Notification

PIANO
Start date: September 2012
Phase: N/A
Study type: Interventional

New York-Presbyterian Hospital has created a system that notifies its primary care providers whenever their patients are admitted to the hospital. In this study, the investigators want to evaluate how accurate this system is and how it is affecting the primary providers and their health care delivery.

NCT ID: NCT01321593 Completed - Emergency Clinical Trials

Hemoglobin Measured by "Orsense NBM-200MP" Device and Laboratory Measurement

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

The purpose of this study is to compare the hemoglobin results obtained with the "Orsense NBM-200MP" device and the Clinical Laboratory.

NCT ID: NCT01281501 Completed - Pain Clinical Trials

Symptomatic Relief of Acute Dyspeptic Pain in Emergency Department With Pantoprazole

Start date: January 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the immediate synergistic effect on the relief of severe acid-related dyspeptic pain by adding intravenous pantoprazole to the combination of oral antacid and antispasmodic agent (the conventional treatment).