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Emergencies clinical trials

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NCT ID: NCT02124356 Completed - Clinical trials for Emergency High-risk Abdominal Surgery

Functional Performance Following Emergency High-risk Abdominal Surgery

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

Emergency abdominal surgery is associated with high mortality rates, multiple postoperative complications and prolonged duration of hospital admission. The purpose of this study is to examine the postoperative functional performance in patients undergoing Emergency High-risk Abdominal Surgery. The hypothesis is that the study can describe the patient population in relation to postoperative functioning, degree of inactivity and the factors that limit mobility.

NCT ID: NCT02116439 Completed - Emergency Room Clinical Trials

Evaluation of the Manifestation of Patient Aggresivity in an Emergency Department

ASAU
Start date: November 2015
Phase: N/A
Study type: Observational

The main objective of this study is to determine the average total number of violent events per observation period occurring in the emergency department at the Nîmes University Hospital. The list of violent events is pre-determined and based on a series of interviews with emergency department staff.

NCT ID: NCT02106325 Completed - Depression Clinical Trials

Ketamine as a Rapidly-Acting Antidepressant in Depressed Emergency Department Patients

Start date: December 2013
Phase: Phase 2
Study type: Interventional

Investigators will conduct a trial to evaluate the use of Ketamine as an alternate treatment for people with Major Depressive Disorder. This study plans to explore the potential that Ketamine's rapid antidepressant action holds for improving outcomes in patients presenting to the Emergency Department with severe depression. Since this is a controlled trial we will use an IV of Ketamine or and equivalent volume of Diphenhydramine. Subjects will be randomly assigned to receive Ketamine or Benadryl. Investigators will then compare measures of mood pre- and post-infusion in the Emergency Department. To supplement self-reported measures of depressive symptoms(e.g. mood), investigators will obtain objective measures of the biological aspects of Major Depressive Disorder.

NCT ID: NCT02104609 Completed - Obesity Clinical Trials

Effects of Obesity on Pharmacokinetics of the Levonorgestrel Emergency Contraceptive Pill

Start date: April 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to determine the effects of obesity on the pharmacokinetics of the levonorgestrel (LNG) only emergency contraceptive (EC) regimen and on markers of ovulation Primary hypothesis: 1) Obese users of LNG-EC have a pharmacokinetic profile that is consistent with a larger volume of distribution of LNG. Secondary hypothesis: 1. Alterations in these pharmacokinetic parameters of the LNG-EC regimen in obese women affect the primary mechanism of action, which is inhibition of ovulation. 2. Obesity may affect other factors that alter levels of LNG, such as sex-hormone binding globulin (SHBG) and albumin, which bind LNG and potentially lowers the amount of free LNG.

NCT ID: NCT02101424 Completed - Overdose Clinical Trials

Monitoring of Overdose Patients With and Without Supplemental Oxygen in the Emergency Department

Start date: May 2010
Phase: N/A
Study type: Observational

This study will compare the data from pulse oximeters to capnographers as they are used to monitor patients who are being observed in the Emergency Department for a suspected overdose of alcohol or other drugs. The investigators will compare monitor data from patients who are and are not on supplemental oxygen, the ability of the monitors to predict the occurrence of airway interventions, and to detect ventilator changes noted on the opposing monitor. There will not be any interventions during this study other than the collection of data from the monitors and observation of the care of patients.

NCT ID: NCT02099227 Completed - Clinical trials for Soft Tissue Infection

Comparative Effectiveness of Emergency Ultrasound Guided Management of Pediatric Soft Tissue Infections

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

To examine the effect of Point-of-Care Ultrasound (POCUS) management guidance on pediatric skin and soft tissue infections treatment failure rate, as well as emergency department process outcome.

NCT ID: NCT02095366 Completed - Clinical trials for Severe Traumatic Pain

Intra Nasal Sufentanil Versus Intravenous Morphine for Acute Severe Traumatic Pain Analgesia in Emergency Setting

ALGOFINE-2
Start date: August 2, 2013
Phase: Phase 4
Study type: Interventional

Intranasal (IN) administration of opiates is an appealing non-invasive way of treating acute traumatic pain in prehospital and Emergency departments (ED). The investigators hypothesize that IN administration of Sufentanil is equal as compared with Intra veinous (IV) administration of Morphine wich is widely recommended in ED. The investigators study is a multicentric, comparative, randomized, double-blind, double-placebo study, comparing quality of analgesia in both groups 30 minutes after first administration of opiates. The investigators also asses side effects and patient satisfaction in both groups.

NCT ID: NCT02094404 Completed - Triage of Children Clinical Trials

Triage of Children at the Emergency Department: Manchester Triage System or Pediatric Early Warning Score?

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

Currently, the Manchester Triage System (MTS) is used to triage all children presenting at the emergency department(ED) in this hospital. This system has been proven safe, but many patients are classified as too urgent. In this hospital adults are prioritised at the ED by a score based on vital signs, the early warning score. A similar score is developed suitable for children. This score, the Pediatric Early Warning Score (PEWS), is already used to determine clinical deterioration. The investigators hypothesize that children can be triaged safely with the PEWS. If it is safe, there will be one triage system again at the ED. Another advantage will be more continuity in assessing the condition of patients who are admitted to the hospital.

NCT ID: NCT02093884 Completed - Pregnancy Clinical Trials

A Pilot Study Using Text Messaging to Communicate With Adolescent Females in the Pediatric Emergency Department

T2I
Start date: January 2014
Phase: N/A
Study type: Interventional

The objective of this study is to develop and test an emergency department (ED)-based intervention which uses text messages to facilitate contraception initiation.

NCT ID: NCT02093078 Completed - Clinical trials for Obstetrical Emergency Situations

Cognitive Aids With Roles Defined (CARD) for Obstetrical Crises: A Multisite Cohort Study

Start date: January 2014
Phase:
Study type: Observational

Crisis resource management represents the set of non technical skills, such as communication, leadership, delegation, and prioritization, that allow effective teamwork for optimal patient care during an urgent and critical situation. The Cognitive Aids with Roles Defined (CARD) is a new concept of cognitive aid addressing the well-documented issue of teamwork in crisis management. It relies on large identification cards specially designed for each team members profession and role. During a life threatening clinical situation, the CARD protocol focuses on clarification of individual roles and distribution of tasks for crisis management rather than creating an additional algorithm identifying either a list of actions to be taken or the dose of a medication. This study aims to evaluate the clinical impact of introducing the CARD protocol in obstetrical emergency situations ("code 333") in clinical practice at The Ottawa Hospital. Hypothesis: CARD protocol will: (i) decrease the total time taken to deliver the baby, and (ii) improve clinical outcome for the mother and baby compared to traditional management without the CARD protocol.