Clinical trials: ED
Acute Vaso Occlusive Crisis (VOC)
L-citrulline Injection in Patients Aged 6-21 Years Old with Sickle Cell Disease Presenting with Vaso-Occlusive Crisis (VOC)
The purpose of this study is to determine if intravenous L-citrulline can abrogate an active vaso-occlusive crisis in sickle cell disease, resulting in decreased pain, reduction or elimination of opiate usage, and reduction or…
- Trial name
- NCT04852172
- Testing
- L-citrulline, D5 1/2NS
- Where
- 2 sites in United States
- Volunteers
- 30 people
- Sponsor
- Asklepion Pharmaceuticals, LLC
Abscess
US Guided Versus BlindI&D for Treatment of Soft Tissue Abscesses in the ED
Standard treatment for a soft tissue abscess involves incision over the area of maximum fluctuance with drainage of purulence from the abscess cavity.
- Trial name
- NCT02264392
- Testing
- Ultrasound Guided Incision and Drainage, Blind Incision and Drainage
- Where
- United States
- Volunteers
- 124 people
- Sponsor
- University of Massachusetts, Worcester
Acute Ischemic Stroke Related to Tandem Occlusion, Acute Ischemic Stroke Due to Isolated Cervical Artery Occlusion
Risk Factors and Outcomes of Ischemic Stroke Associated With Tandem or Isolated Cervical Artery Occlusion in Anterior and Posterior Circulation
CERES-TANDEM is a multicenter study designed to improve the understanding of "tandem" ischemic stroke -those caused by two blockages in series, one in a neck artery and one in a brain artery-.
- Trial name
- CERES-TANDEM (NCT06965036)
- Where
- 3 sites in United States, Italy and 1 more
- Volunteers
- 4,230 people
- Sponsor
- Azienda Unità Sanitaria Locale della Romagna
Emergency Care, Clinical Decision Support
Artificial Intelligence(AI) in the Emergency Department (ED) in Cologne
This retrospective, non-interventional study evaluates the prognostic performance of open-weight Large Language Models (LLMs) in the setting of a German academic emergency department.
- Conditions
- Emergency Care, Clinical Decision Support, Triage
- Trial name
- KINA-CO (NCT07725965)
- Where
- Germany
- Volunteers
- 100,000 people
- Sponsor
- University of Cologne
All Eligible ED Patients (Not Limited to a Particular Condition)
Juice Preference in the Emergency Department
ED patients who are able to drink juice will be approached and asked their beverage preference.
- Trial name
- JUICED (NCT02506478)
- Testing
- Beverage procurement
- Where
- United States
- Volunteers
- 385 people
- Sponsor
- Hennepin Healthcare Research Institute
Atrial Fibrillation, Atrial Flutter
Decreasing Hospital Admissions From the ED for AAFF
Acute atrial fibrillation and flutter (AAFF) is characterized by rapid heart rates with onset less than seven days. It's the most common type of palpitation treated in the Emergency Department (ED).
- Trial name
- RAFF-3 (NCT03627143)
- Testing
- KTI activities
- Where
- 12 sites in Canada
- Volunteers
- 846 people, healthy volunteers welcome
- Sponsor
- Ottawa Hospital Research Institute
Wheezing, Bronchiolitis
Bedside Lung Ultrasound in Young Children Presenting to the Emergency Department (ED) With Wheezing
Young children presenting to the Emergency Department (ED) with wheezing often have prolonged stays in the ED or even get admitted to the hospital.
- Trial name
- NCT01452945
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- Children's National Research Institute
School Difficulties Associated With Mental Health Problems
Partnerships Between Schools and Public Mental Health Departments: Investigation of Multi-professional Interventions for Children Aged 3 to 8 With Mental Health Issues (Parpsych-Ed)
Local partnerships between schools (preschool and elementary) and mental health public services are implemented in seven sites in France.
- Trial name
- Parpsych-Ed (NCT04300712)
- Testing
- Questionnaires at the start and end of the school year
- Where
- 7 sites in France
- Volunteers
- 2,000 people, healthy volunteers welcome
- Sponsor
- GCS pour la recherche et la formation en sante mentale
Acute Asthma
Emergency Department (ED)-Directed Interventions to Improve Asthma Outcomes
The purpose of this study is to determine if evidence-based guidance on follow-up care and self-management provided to PCPs and patients, respectively, reduces relapses within 90 days for acute asthma (primary outcome).
- Trial name
- NCT01079000
- Testing
- Opinion Leader letter, Involvement of a care manager, Usual care
- Where
- 2 sites in Canada
- Volunteers
- 367 people
- Sponsor
- University of Alberta
Eating Disorder
An ACT Group Intervention for ED-patients
The purpose of this study was to test if an ACT group intervention focusing on body image reduces eating disorders symptoms and reduces care consumption in patients treated at a specialised eating disorder unit.
- Trial name
- NCT02058121
- Testing
- Acceptance and Commitment Therapy, Treatment as usual
- Where
- Sweden
- Volunteers
- 99 people
- Sponsor
- Örebro County Council
Atrial Fibrillation
hsTnT in Patients Admitted to the ED With Atrial Fibrillation in the Era of NOACs - Heidelberg Registry of Atrial Fibrillation
The purpose of the Heidelberg Registry of Atrial Fibrillation (HERA-FIB) is to collect data on the prevalence and clinical significance of elevated cardiac troponin in a large registry of unselected patients with atrial…
- Trial name
- HERA-FIB (NCT03344237)
- Where
- Germany
- Volunteers
- 5,000 people
- Sponsor
- University Hospital Heidelberg
Muscular Dystrophies, Muscle Inflammation
Safety and Efficacy of a Flavonoids- and omega3s-based Compound for the Treatment of Muscular Dystrophies
The study aimed to assess the safety and, partially, the efficacy of dietary supplementation of a flavonoids-, DHA- and EPA-based natural supplement in non-ambulant DMD boys and in a cohort of LGMD and FSHD patients to compare…
- Trial name
- PRO1 (NCT03317171)
- Testing
- Flavonoids, DHA, EPA
- Where
- Italy
- Volunteers
- 29 people
- Sponsor
- Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico