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Emergencies clinical trials

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NCT ID: NCT04715854 Active, not recruiting - Covid19 Clinical Trials

Effect on paO2 of Adding an Aerosol Mask Above the Nasal Canulas

Start date: February 19, 2021
Phase: N/A
Study type: Interventional

This study will compare the impact of a classical aerosol mask above low-flow nasal cannula on the arterial oxygen tension in patients with COVID-19.

NCT ID: NCT04678817 Active, not recruiting - Contraception Clinical Trials

Same Day Oral EC and Implant Initiation

Start date: January 15, 2021
Phase:
Study type: Observational

This is a study for clients presenting for emergency contraception (EC). EC is used to prevent pregnancy after unprotected intercourse. Clients presenting for EC may be offered either the copper or hormonal IUD or oral EC. Current guidelines allow for same-day implant initiation at the time of an EC encounter, as long as oral LNG EC is co-administered. This study will look at pregnancy rates and clients willingness to receive same-day implant + oral EC and same-day IUDs.

NCT ID: NCT04648449 Active, not recruiting - Stroke, Acute Clinical Trials

Artificial Intelligence (AI) Support in Medical Emergency Calls

AISMEC
Start date: September 1, 2020
Phase:
Study type: Observational

More than 12.000 patients suffer acute stroke in Norway every year, but less than half of them reach hospital within the current treatment window for thrombolysis. Stroke is the third-highest cause of death and the number one cause of severe disability requiring long time care at institutions. Consequently this has a high impact on society, patients and relatives, in addition to high costs related to care estimated to approximately 10 billion NOK per year. Although there are few studies on emergency medical communication centres (EMCC) in Norway, some have shown that the performance of the emergency medical communication centres can be improved. This project will seek to amend EMCC´s handling of acute stroke inquiries using artificial intelligence (AI), thus contributing to getting the patient to hospital in time for optimal treatments.

NCT ID: NCT04611295 Active, not recruiting - Emergencies Clinical Trials

TELENeurological Support for Emergency Department

TELENS-ED
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

Open-label, non-inferiority, teleconsultation with televisit study to compare efficacy, safety and users satisfaction of a TeleNeurological Support versus "in person" neurological examination in the emergency department

NCT ID: NCT04550169 Active, not recruiting - Clinical trials for Emergency Department Visit

Wisconsin Evaluation of Emergency Department Care Coordination

Start date: March 1, 2022
Phase:
Study type: Observational

The State of Wisconsin is now expanding its investment in care coordination models as an effort to reduce inappropriate hospital emergency department (ED) use, improve health outcomes, and reduce Medicaid expenditures. This effort begins with a pilot program to support emergency department care coordination in hospitals and health systems that apply and are selected to participate in the pilot program. The Wisconsin Medicaid program seeks to understand whether this program achieves its intended goals and, specifically, whether the Medicaid payment for such care coordination services produces the intended program outcomes. Hospitals will select members that will receive care coordination services. In a quasi-experimental approach, the study team will compare members that do vs. do not receive the services will be used examine the effects of care coordination and referrals on total ED visits, primary-care treatable ED visits, non-emergent ED visits, and health care costs, as well as the specific effects of referring patients to providers who offer low-cost and after-hours care. To assess the importance of targeting, study team will conduct stratified analyses of vulnerable groups such as people with disabilities and individuals with specific clinical needs.

NCT ID: NCT04540094 Active, not recruiting - Sepsis Clinical Trials

Feasibility of 5% Albumin Compared With Balanced Crystalloid, as Intravenous Fluid Resuscitation in Adult Patients With Sepsis, Presenting as an Emergency to Hospital

ABC Sepsis
Start date: June 1, 2021
Phase: Phase 3
Study type: Interventional

The aim of this research study is to compare two different fluids (Human Albumin Solution (HAS) and Balanced Crystalloid that are given via a drip to patients with severe infection (sepsis). The investigators plan to see which fluid is better, and to see if they have a role in improving a patient's recovery time, reducing complications and the length of time they stay in hospital. This study plans to find out if there is evidence that one fluid is better overall to determine the need for a subsequent definitive trial.

NCT ID: NCT04533698 Active, not recruiting - Resternotomy Clinical Trials

Impact of Fluid Resuscitation Protocol on the Incidence of Reoperation for Bleeding After Emergency Cardiopulmonary Bypass Grafting

Volu-CABG
Start date: January 1, 2009
Phase:
Study type: Observational

This is a retrospective data analysis of patients that underwent elective or emergency cardiopulmonary bypass. Resternotomy due to bleeding is frequent after sternotomy. Also due to implementation of Argipressin into clinical practice fluid resuscitation protocol has changed to more vasopressors and less fluid within the past five years. The investigators want to explore the influence of volume resuscitation protocol on incidence of rethoracotomy during the past twenty years.

NCT ID: NCT04409535 Active, not recruiting - Mental Health Issue Clinical Trials

Effects of the COVID-19 Health Emergency on Biopsychosocial Health

Start date: May 7, 2020
Phase:
Study type: Observational

There is a critical need to determine the impact of the COVID-19 emergency on the comprehensive well-being of people as they are living through the emergency and sequelae of the emergency period. The research team is requesting National Institutes of Health funding with the goal to investigate rural vs. urban living people's response to the crisis and its impact using mixed methods research.

NCT ID: NCT04311788 Active, not recruiting - Incisional Hernia Clinical Trials

Preemer Trial - Prophylactic Mesh Versus no Mesh in the Midline Emergency Laparotomy Closure for Prevention of Incisional Hernia: a Multi Center, Double-blind, Randomized Controlled Trial

Start date: April 27, 2020
Phase: N/A
Study type: Interventional

244 patients, who have an emergency midline laparotomy for any gastrointestinal reason, will be randomized in a 1:1 ratio either to mesh group with a retrorectus prophylactic self-gripping mesh or to control group with 4:1 small stitch closure by continuous monofilament suture. They will be followed up at 30 days, 2 and 5 years to detect the incidence of incisional hernia.

NCT ID: NCT04304495 Active, not recruiting - Fall Clinical Trials

The Geriatric Acute & Post-acute Care Coordination Program for Fall Prevention in the Emergency Department II

GAPcareII
Start date: January 6, 2021
Phase: Phase 2
Study type: Interventional

In brief, this K76 study consists of a small open trial to refine the study protocol and train study personnel on study procedures (Aim 1.b.). In Aim 2, we will recruit older adults into a multidisciplinary fall prevention pilot study. Participants will be randomly assigned to usual care with a traditional fall evaluation by an ED clinician (i.e., ED medical staff member) or an intervention. In the intervention, participants will receive an in-ED consultation by a physical therapist and pharmacist to determine reasons for the fall and offer additional education and training. Participants will be provided an Apple Watch to record measures of fitness and falls, if possible, in the following 12 months. Recurrent falls will be measured in twelve-month follow-up.