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Emergencies clinical trials

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NCT ID: NCT03293862 Completed - Clinical trials for Surgical Wound Dehiscence

Prevention of Fascial Dehiscence With Prophylactic Onlay Mesh in Emergency Laparotomies

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

Facial dehiscence elicit high morbidity and mortality. This complication may arise in more than 8.5% of high-risk patients. Addressing risk factors and optimizing surgical technique are guarded as mainstay measures for prevention, but their efficacy is questionable. The aim of this study is to analyze the influence of using a polypropylene onlay prophylactic mesh on the incidence of fascial dehiscence in emergency surgery and associated complications.

NCT ID: NCT03293160 Completed - Clinical trials for High Utilization of Emergency Departments

An Evaluation of the Michigan State Innovation Model in Washtenaw and Livingston Counties

Start date: November 1, 2017
Phase:
Study type: Observational

This study will examine the effects of a care management program on the health and health spending outcomes of patients residing in Michigan's Washtenaw and Livingston Counties.

NCT ID: NCT03286179 Completed - Clinical trials for Acute Coronary Syndrome

Standardizing Emergency Work-ups Around Risk Data

STEWARD
Start date: July 1, 2018
Phase:
Study type: Observational

Chest pain is the second leading reason for emergency department (ED) visits in the United States. Resource utilization for this ED subpopulation is particularly high, in part due to a dearth of accepted standardized clinical approaches and general overestimation of risk on the part of both providers and patients. This prospective observational cohort study seeks to address this issue by providing externally validated risk scores for major adverse cardiac events using a web-based clinical decision support platform (RISTRA) embedded within the electronic health record at 13 Kaiser Permanente Northern California (KPNC) EDs over a 12-month period. The decision support will provide risk estimates specific to the KPNC patient population. This studies hypothesis is that the provision of more accurate risk estimation for major adverse cardiac events will improve informed decision making by both providers and patients, resulting in less provocative testing and lower ED lengths of stay amongst low risk patients, as well as improving medical management among non-low risk patients and decreasing future rates of major adverse cardiac events.

NCT ID: NCT03270930 Completed - Emergencies Clinical Trials

Operative Duration as a Predictor of Mortality in Pediatric Emergency Surgery

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

Introduction Operative duration is an important but under-studied predictor of mortality in emergency laparotomies. Aims & Objectives The objective of this study was to quantify the effect of duration of emergency laparotomy in children on mortality and to identify a rough cut-off duration of laparotomy to serve as a guide to plan the laparotomy to optimize pediatric surgical patient outcome.

NCT ID: NCT03262025 Completed - Laparotomy Clinical Trials

Primary Cecal Pathologies Presenting as Acute Abdomen

Start date: January 1, 2016
Phase: N/A
Study type: Observational

Background: The importance of cecal pathologies lie in the fact that being the first part of large intestine, any disease involving the cecum affects overall functioning of the large bowel. Primary cecal pathologies presenting as acute abdomen have not been described in any previous study in terms of presentation, management and outcome. Objectives: The objective of this study was to identify the reported causes of primary cecal pathologies presenting as acute abdomen and the various causes presenting in Indian setting, to discuss morbidity and mortality associated with cecal pathologies and to critically analyse the various management modalities employed in emergency setting.

NCT ID: NCT03261648 Completed - Anxiety Clinical Trials

Anxiety of Patient and His Partner During Admission to Emergency Department

ANXURG
Start date: May 23, 2017
Phase: N/A
Study type: Observational

Evaluate and compare the impact of partner's stress in the pain of the patient admitted in the emergency department

NCT ID: NCT03258073 Completed - Clinical trials for Maternal, Pediatric Care Emergencies

Does Simulation Scenario Execution Improve Acute Care Skills and Confidence Related to Maternal and Pediatric Care Emergencies?

SimForLife
Start date: August 30, 2017
Phase: N/A
Study type: Interventional

In Uganda and many countries in Sub-Saharan Africa, health providers have minimal training and intermittent opportunity to maintain skills in managing delivery complications and acute newborn and pediatric conditions. Interventions like effective resuscitation assistance at the time of birth are lifesaving. Every 30 second delay in establishing effective resuscitation at birth increases the risk of death by 16%. The purpose of this study is to test whether medical simulation can improve acute care skills and confidence related to maternal and pediatric care emergencies.

NCT ID: NCT03256903 Completed - Clinical trials for Acute Pain Due to Trauma

Methoxyflurane vs Standard Analgesic Treatment for Trauma Pain in Spanish Emergency Units

InMEDIATE
Start date: July 7, 2017
Phase: Phase 3
Study type: Interventional

Clinical trial to compare pain relief between methoxyflurane and any analgesic treatment used in usual clinical practice, in patients with trauma and associated pain, treated in Spanish emergency units.

NCT ID: NCT03255772 Completed - Clinical trials for Myocardial Infarction

Magnetocardiography Using a Novel Analysis System (Cardioflux) in the Evaluation of Emergency Department Observation Unit Chest Pain Patients

Start date: July 15, 2017
Phase:
Study type: Observational

Genetesis is a cardiac diagnostics company which presents a novel magnetocardiogram (MCG) analysis system called CardioFlux. This investigation presents a new, noninvasive diagnostic option to use MCG for rapid diagnosis of acute coronary syndrome. Data from the Cardioflux system will be compared with stress testing methods as well as the results of cardiac catheterization to identify patients with myocardial ischemia. This is a prospective observational single-blinded convenience pilot study of 100 patients placed in the Clinical Decision Unit (CDU) for evaluation of chest pain at St. John Hospital and Medical Center (Detroit, MI). Patients enrolled in the study will also have a 30 and 180 day follow up for analysis of adverse cardiac events.