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Emergencies clinical trials

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NCT ID: NCT01402635 Completed - Crowding Clinical Trials

Can the Point-Of-Care Chemistry Test (POCT) Solve the Emergency Department (ED) Crowding?

POCTED
Start date: January 2011
Phase: N/A
Study type: Interventional

The hypothesis of this study that the Point-Of-Care Chemistry Test (POCT) may shorten Emergency Department (ED) length of stay (LOS).

NCT ID: NCT01401816 Completed - Sexually Active Clinical Trials

Advanced Provision of Emergency Contraception: Utilizing Technology to Increase Prescription Fill Rates

Start date: July 2011
Phase: N/A
Study type: Interventional

Eighty-five percent of the 750,000 teenage pregnancies per year in the United States are unintended (Guttmacher Institute). Approximately half of all teenage pregnancies end in the birth of a child; the remaining proportion end in either abortion (30%) or miscarriage (20%). It has been estimated that if Emergency Contraception (Plan B) was used after every contraception failure, it could prevent 50% of unintended pregnancies and 60-70% of abortions annually. Previous studies have showed the effectiveness of emergency contraception decreases with time after intercourse; the sooner it is taken—even if it means a matter of hours—the more effective it is in preventing pregnancy. Based on previous studies, it is clear that relying on obtaining emergency contraception on the same day or even the day after unprotected intercourse is not guaranteed. For example, approximately 27% of pharmacies called by the adolescent mystery caller did not have the medication available the day of the call and almost all of the pharmacies not stocking the medication would take greater than 24 hours to obtain it through their ordering system. Thus, the concept of advanced provision of emergency contraception has been proposed to assure that the medication can be taken as soon as possible. Although this practice is known to be safe and has not shown any association with increased sexual risk or behaviors, it is unclear how often/if adolescents will fill a prescription for a medication that is not needed at the time of a medical encounter. The investigators propose a randomized pilot study (n=60) of a text-messaging intervention that aims to increase the rate at which prescriptions for emergency contraception are filled. Based on practice norms in the BMC Adolescent Center, sexually active female adolescents (ages 13-21) in both the control and intervention groups will be provided a prescription for emergency contraception. The intervention group, however, will receive follow-up text message on their phone reminding them to fill the prescription. Boston Medical Center Health Plan will provide prescription fill data regarding the prescriptions written at the time of enrollment. Approximately 6 weeks after enrollment, all study participants will be contacted for a follow-up survey.

NCT ID: NCT01392508 Completed - Sepsis Clinical Trials

IMproved PREdiction of Severe Sepsis in the Emergency Department

IMPRESSED
Start date: March 2011
Phase: N/A
Study type: Observational

The purposes of this study is to determine whether Heparin Binding Protein (HBP) can be used as a marker of severe sepsis (including septic shock) in patients presenting to the emergency department with suspected infection.

NCT ID: NCT01388374 Completed - Primary Health Care Clinical Trials

The (Cost-)Effectiveness of Nurse Practitioners Working at the Primary Out of Hours Emergency Service

Start date: December 2010
Phase: N/A
Study type: Interventional

The aim of this study is to explore whether the implementation of Nurse Practitioners can lead to a more accessible and efficient patient care at the primary out of hours service. The primary objectives of the proposed study are: 1. What are the effects of the implementation of NPs on the primary out of hours service in comparison with the current out of hours service? Effects in terms of accessibility, objective and subjective workload of general practitioners, quality of care and patient satisfaction. 2. How efficient is the implementation of NPs in the primary out of hours services? 3. What is the feasibility of the implementation of NPs in the out of hours services? And under which conditions? 4. What are the barriers and facilitating factors considering the implementation of NPs?

NCT ID: NCT01387139 Completed - Clinical trials for Procedural Sedation and Analgesia

Ketamine Versus Co-administration of Ketamine and Propofol for Procedural Sedation in a Pediatric Emergency Department

Start date: January 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness of the co-administration of intravenous ketamine and propofol to intravenous ketamine as a single agent for procedural sedation in the pediatric emergency department. The investigators hypothesize that patients receiving co-administration of ketamine and propofol will have a lower rate of adverse events, compared to patients receiving ketamine for procedural sedation.

NCT ID: NCT01384448 Completed - Clinical trials for Coronary Artery Disease

Stress Echocardiography and Heart Computed Tomography (CT) Scan in Emergency Department Patients With Chest Pain

Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether stress echocardiography or computed tomography (CT) of the heart is better at diagnosing emergency room chest pain patients to select appropriate candidates for hospitalization and further work-up.

NCT ID: NCT01376414 Completed - Peptic Ulcer Clinical Trials

H. Pylori Testing for Patients With Non-specific Upper Abdominal Pain in the Emergency Department

Start date: March 2011
Phase: N/A
Study type: Observational

This pilot study aims to estimate the prevalence of Helicobacter pylori (H. pylori) colonization in patients presenting with non-specific abdominal pain (NSAP) in an urban academic emergency department (ED) located in Washington, DC.

NCT ID: NCT01375634 Completed - Clinical trials for Intubation; Difficult

Nasogastric Tube Insertion Using Midazolam in the Emergency Department

NIMED
Start date: May 2011
Phase: Phase 4
Study type: Interventional

Nasogastric tube placement involves insertion of a flexible tube through the nose into the stomach. Placement of the tube can irritate the nose and palate and trigger gagging, causing discomfort, even if topical or local anesthetics are used. This study aims to determine if administration of an ultra-short acting sedative agent (midazolam) into a vein before the procedure, in addition to topical local anesthetic, will decrease the level of discomfort.

NCT ID: NCT01374295 Completed - Clinical trials for Non-critical Emergency Room Patients Receiving Lortab Medication or Prescription During Their Emergency Room Visit

Video Assisted Informed Consent for Lortab to Improve Patient Satisfaction and Knowledge

Start date: March 2011
Phase: N/A
Study type: Interventional

In order to compare two different forms of patient education; patients who receive Lortab medication or prescription during their ED visit are randomized to receive either standard patient education (from healthcare provider) or video assisted education. After education, patient completes a survey, estimated to take 5 minutes to complete.

NCT ID: NCT01373775 Completed - Clinical trials for Congestive Heart Failure

Risk Factors of the Revisit of the Adult Heart Failure Patients in Emergency Department Siriraj Hospital

Start date: April 2009
Phase: N/A
Study type: Observational

To identify the risk factors of the revisit of the adult HF patients in emergency department.