Clinical trials: Emergency Departments
IUD, Contraceptive Implant
Quick Start of Highly Effective Contraception
This project will quantify rates of contraceptive failure when unprotected intercourse occurs 6-14 days prior to initiation of highly effective reversible contraceptives (such as IUD's and Implants).
- Conditions
- IUD, Contraceptive Implant, Contraception, Birth Control
- Trial name
- NCT02076217
- Testing
- Copper T-380 IUD, LNG IUD, Contraceptive implant Nexplanon
- Where
- United States
- Volunteers
- 270 people
- Sponsor
- University of Utah
Small Bowel Obstruction, Point of Care Ultrasound
POCUS for Small Bowel Obstruction in the ED: a Retrospective Study
This study protocol aims to evaluate the impact of point-of-care ultrasound (POCUS) on the diagnosis and management of small bowel obstruction (SBO) in the emergency department (ED).
- Trial name
- SBOCUS (NCT05864378)
- Volunteers
- 230 people
- Sponsor
- Azienda Ospedaliero-Universitaria di Modena
Acute Pain
OMT vs. Standard Therapy in the Management of Acute Neck and Low Back Pain in the Emergency Department
Patients 18 to 65 years old who present within 72 hours of onset pain will be considered for study enrollment. Patients with the acute musculoskeletal low back or neck pain based on ED history and structural physical exam will be…
- Trial name
- NCT06987578
- Testing
- OMT vs. Ibruprofen
- Where
- United States
- Volunteers
- 45 people
- Sponsor
- St. Joseph's Regional Medical Center, New Jersey
Anaphylaxis, Hypoxia
Virtual Reality-Based Simulation Versus High-Fidelity Simulation for Emergency Management Training in Medical Interns
This study is a two-arm parallel randomized controlled non-inferiority trial designed to compare the educational effectiveness of virtual reality (VR)-based simulation with high-fidelity simulation (HFS) for emergency management…
- Trial name
- NCT07584863
- Testing
- Virtual Reality-Based Emergency Simulation, High-Fidelity Simulation
- Where
- South Korea
- Volunteers
- 124 people, healthy volunteers welcome
- Sponsor
- Seoul National University Hospital
Latent Tuberculosis, Active Tuberculosis
Improving the Detection of Active Tuberculosis in Accident and Emergency Departments
Tuberculosis (TB) control remains a public health challenge. Many people in the UK do not have a general practitioner (GP) registration and their only interaction with the NHS is via Accident and Emergency (A\&E) Departments of…
- Trial name
- ACE (NCT02512484)
- Testing
- venepuncture, sputum collection, xray
- Where
- 3 sites in United Kingdom
- Volunteers
- 1,000 people, healthy volunteers welcome
- Sponsor
- Public Health England
Malaria
Insecticide Treated Polyethylene Sheeting for Prevention of Malaria in Emergencies
A Phase III malaria prevention trial was conducted in two camps of Liberian refugees in Sierra Leone using Insecticide Treated Polyethylene Sheeting (ITPS) or untreated polyethylene sheeting (UPS) randomly deployed to defined…
- Trial name
- NCT01456858
- Testing
- Insecticide Treated Polyethylene Sheeting, Untreated Plastic Sheeting
- Where
- Sierra Leone
- Volunteers
- 222 people, healthy volunteers welcome
- Sponsor
- The Mentor Initiative
PARKINSON DISEASE (Disorder)
Description of the Reasons for Hospitalization of Patients With Parkinson's Disease Following Admission Through the Adult Emergency Department
The goal of this observational study is to investigate the causes of hospitalisation via emergency services in patients with degenerative parkinsonian syndromes.
- Trial name
- Emerge Park (NCT07439926)
- Testing
- No Intervention: Observational Cohort
- Where
- France
- Volunteers
- 2,580 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Malignant Hypertension
Determinants of Malignant Hypertension Onset and Related Target Organ Damages: the HAMA Biobank
The HAMA bank is an initiative aimed at collecting, preparing, and storing biological samples from patients treated for malignant hypertension and included in the HAMA cohort.
- Trial name
- HAMABANK (NCT06629363)
- Testing
- biobank
- Where
- 11 sites in France
- Volunteers
- 1,000 people
- Sponsor
- Centre Hospitalier de PAU
Length of Admission
Predictors for Admission to Emergency Department More Than 48 Hours
In Demark acutely admitted patients are supposed to stay in the Emergency Department (ED) bed ward if the anticipated duration of stay is less than 48 hours.
- Trial name
- NCT01723449
- Where
- Denmark
- Volunteers
- 730 people
- Sponsor
- University of Southern Denmark
Emergency Department, Length of Stay
Point-Of-Care Chemistry Test (POCT) Effect on the Emergency Department (ED)
The hypothesis of this study is that POCT will shorten ED turn-around-time (TAT) such as blood drawing TAT, lab TAT, and decision TAT.
- Conditions
- Emergency Department, Length of Stay, Turnaround-time
- Trial name
- NCT00942955
- Sponsor
- Seoul National University Hospital
Pain
Comparing Intravenous Hydromorphone to Usual Care
In this randomized controlled trial, 2 mg intravenous (IV) hydromorphone will be more efficacious than usual care (usual care is analgesic management according to the judgment of the attending physician caring for that patient)…
- Trial name
- NCT01429298
- Testing
- Hydromorphone, Usual care
- Where
- United States
- Volunteers
- 350 people, healthy volunteers welcome
- Sponsor
- Montefiore Medical Center
Angina, Unstable
Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Testing on Outcomes
In a randomized, controlled clinical trial, point-of care testing at the bedside using the cardiac biomarker troponin I in ED patients with possible ACS will be compared to traditional testing of this assay for myocardial…
- Trial name
- Dispo-ACS (NCT00222352)
- Testing
- Point of Care cTnL testing
- Where
- 4 sites in United States
- Volunteers
- 2,000 people
- Sponsor
- University of Cincinnati
Upper Gastrointestinal Bleeding
Single-use Versus Reusable Gastroscopes in Patients With Upper Gastrointestinal Bleeding.
Controlled-randomized trial evaluating single-use versus reusable gastroscopes in patients with upper gastrointestinal bleeding.
- Trial name
- OneScopeII (NCT06192355)
- Testing
- Endoscopic hemostasis using a Esophagogastroduodenoscopy
- Where
- Germany
- Volunteers
- 150 people
- Sponsor
- University Hospital Augsburg
Fractures, Bone
Fracture In Preterm Infants Study (FIPIN Study)
Children who are born early (pre-term infants) are at increased risk of fractures until the age of 2 years, due to their weak bones caused by several physiological, and environmental factors.There is however little information…
- Trial name
- NCT04215315
- Testing
- Retrospective observation
- Where
- United Kingdom
- Volunteers
- 120 people
- Sponsor
- Sheffield Children's NHS Foundation Trust
Soft Tissue Injuries, Gouty Arthritis
AMPED Outcomes Registry of Post-ED Pain Management
Study aims to assess patient-recorded outcomes of pain control medications prescribed in the ER after visits for specific painful injuries/illnesses.
- Conditions
- Soft Tissue Injuries, Gouty Arthritis, Fractures, Ureteral Colic
- Trial name
- AMPED (NCT01626235)
- Where
- 11 sites in United States
- Volunteers
- 843 people
- Sponsor
- Radnor Registry Research, Inc
Emergency Service, Hospital
Nudging High-acuity Emergency Department Patients to Schedule a Follow-up Visit
The goal of this campaign is to reduce unnecessary emergency department (ED) visits by encouraging patients with high acuity visits to follow up with an appropriate primary care provider (PCP) or specialist and therefore obtain…
- Trial name
- NCT06535347
- Testing
- Information about scheduling a follow-up appointment
- Where
- United States
- Volunteers
- 6,814 people
- Sponsor
- Geisinger Clinic
Suicide, Suicidal
Safe Treatment for Emergency Presentation for Suicidal Ideation and Behavior in Youth
This randomized comparative effectiveness trial will compare two evidence-based approaches to emergency care for youth ages 13-24 who present to the Emergency Department (ED) with suicidal ideation or behavior.
- Conditions
- Suicide, Suicidal, Self-Harm
- Trial name
- SAFE STEPS (NCT05304065)
- Testing
- SAFETY-A within usual ED Care, Combined SAFETY-A within usual ED Care + CLASP Therapeutic Follow-Up Contacts
- Where
- 5 sites in United States
- Volunteers
- 1,600 people
- Sponsor
- University of California, Los Angeles
Asthma
Asthma Learning Project
The purpose of this study is to determine the effect on knowledge and behavior of playing an educational asthma computer game during a pediatric Emergency Department (ED) asthma visit among children ages 7 - 15 years.
- Trial name
- ALP (NCT00874900)
- Testing
- Educational game, Educational game + motivational interview, Motivational interview
- Where
- United States
- Volunteers
- 120 people
- Sponsor
- Seattle Children's Hospital
Surgery--Complications, Abdomen Disease
Use of Wearables for Early Detection of Complications After Major Acute Abdominal Surgery
The purpose of the study is to investigate whether glucose profile, sleep disturbances and heart rate variability measured with wearable devices is associated with postoperative recovery and complications within 30 days after…
- Trial name
- NCT04257344
- Where
- Denmark
- Volunteers
- 40 people
- Sponsor
- Zealand University Hospital
Older Adults (65 Years and Older), Fall Prevention
Modifying the Geriatric Acute & Post-acute Care Coordination Program for Fall Prevention in the Emergency Department for Telehealth
The goal of this clinical trial is to determine the feasibility of eGAPcare, a telehealth modification of the GAPcare fall prevention intervention, in older adults in a community emergency department.
- Conditions
- Older Adults (65 Years and Older), Fall Prevention, Telehealth, Emergency Department
- Trial name
- eGAPcare (NCT07034287)
- Testing
- Telehealth physical therapy and pharmacy consultation
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- University of Colorado, Denver
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