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Emergencies clinical trials

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NCT ID: NCT02308696 Completed - Hospitalization Clinical Trials

The Effectiveness of Peer-to-Peer Community Support to Promote Aging in Place

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

The investigators' overall objective is to evaluate the effectiveness of peer-to-peer support programs in preventing the necessity of acute health care and nursing home services for older adult populations and in promoting their health and wellness. The investigators' Specific Aims are: 1. To compare the effectiveness of peer-to-peer community support in preventing hospitalization, emergency department (ED) use, and nursing home placement in an at-risk older adult population relative to standard community services. 2. To compare the effect of peer-to-peer community support on intermediary measures of health and wellness such as self-rated health, depression, and anxiety relative to standard community services.

NCT ID: NCT02307136 Completed - Clinical trials for Intensive Care Units

Evaluation of the Impact of Within-hospital Trajectories of Patients Admitted in Intensive Care Units (ICU) From Emergency Departments

SUREA
Start date: January 2013
Phase: N/A
Study type: Observational

This multicenter cohort aims to assess the impact of within-hospital trajectories of patients admitted in intensive care units from emergency departments on vital prognosis of patients, duration of hospital stay and hospital costs. As secondary objectives, the study will: - assess the impact of clinical and demographic characteristics on hospital trajectories of patients. - assess the impact of emergency units workload, beds availability in medical units and in intensive care units, and global hospital organisation on patients care trajectories.

NCT ID: NCT02299024 Completed - Clinical trials for Opioid Use, Unspecified

Prescribing Opioid Pain Relievers in the Emergency Department: Understanding and Optimizing the Encounter

Start date: October 2012
Phase: N/A
Study type: Interventional

The investigators overall study objective is to improve patients knowledge and safe use of opioid pain relievers upon discharge from the Emergency Department.

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: NCT02296866 Completed - Emergency Surgery Clinical Trials

Assessment of Prokinetic Effects of Erythromycin in Emergency Patients With a Full Stomach

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

The aims of the study is to assess whether the intravenous infusion of 3 mg/kg erythromycin has a significant gastrokinetic effect leading to empty the stomach in less than 90 minutes in non-fasting patients undergoing emergency trauma surgery.

NCT ID: NCT02286479 Completed - Skin Abscess Clinical Trials

Comparison of Loop and Primary Incision&Drainage Techniques in the Emergency Department

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

Skin abscesses are among the most common soft tissue infections cause emergency room visits frequently. Management of abscess drainage and prevent further complications are important entities for emergency physicians. Historically primary incision and drainage (I&D) technique has found very effective method of abscess drainage, however a novel technique loop drainage holds promising. The purpose of our study is comparison efficacy of I&D and loop drainage techniques in patients with cutaneous abscess.

NCT ID: NCT02273687 Completed - Clinical trials for Respiratory Distress Syndrome, Adult

Time-motion-mode Ultrasound Diaphragm Measures in Patients With Acute Respiratory Distress in Emergency Department

EDDRAPro
Start date: October 29, 2014
Phase: N/A
Study type: Interventional

The main objective of this study is to show that "diaphragmatic excursion measures upon emergency admission" (CDA values) on patients with acute respiratory failure are predictive of the need to use mechanical ventilation (invasive or non-) in the first four hours.

NCT ID: NCT02269098 Completed - Clinical trials for Diabetes Mellitus, Type 2

The Synergy to Control Emergency Department Hyperglycemia Program for Type 2 Diabetes

STEP-DM
Start date: February 2012
Phase: N/A
Study type: Interventional

A 4 week prospective, randomized controlled study was carried out to assess the impact of a care delivery intervention which focused on blood glucose (BG) management among adults with type 2 diabetes presenting to the Emergency Department (ED) with BG >/= 200mg/dL (11.1 mmol/L). The intervention was designed by a multi-disciplinary team of ED physicians and nurses, endocrinologists and diabetes educators. The intervention incorporated three components: a guideline-based algorithm for diabetes medication management survival skills diabetes self-management education (DSME); and support for health system navigation. The control group received usual care per the ED's policies and procedures for management of high blood glucose.

NCT ID: NCT02268877 Completed - Pregnancy Clinical Trials

A Randomized Prospective Analysis of Time to Diagnosis and Length of Stay of Emergency Department Pelvic Ultrasonography

Start date: March 2013
Phase: N/A
Study type: Interventional

The goal of this project is to compare the efficiency of pelvic ultrasounds performed by emergency medicine residents and attending physicians to the efficiency of pelvic ultrasounds performed by the department of radiology.

NCT ID: NCT02248753 Completed - Atrial Fibrillation Clinical Trials

Acute Cardioversion Versus Wait And See-approach for Symptomatic Atrial Fibrillation in the Emergency Department

RACE 7 ACWAS
Start date: October 2014
Phase: N/A
Study type: Interventional

A symptomatic episode of the heart rhythm disorder 'atrial fibrillation' (AF) is a frequent reason for visits to the emergency department. Currently, in the majority of cases, immediate (electrical or pharmacological) cardioversion is chosen, while atrial fibrillation terminates spontaneously in 70% of the cases within 24 hours. A wait-and-see approach with rate-control medication only, and when needed cardioversion within 48 hours of onset of symptoms, could be effective, safe and more cost-effective than current standard of care and could lead to a higher quality of life.