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Emergencies clinical trials

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NCT ID: NCT02534324 Completed - Hypertension Clinical Trials

The Effect of Pre-discharge Blood Pressure of Patients With Asymptomatic Severe Hypertension in Emergency Department

Start date: September 2015
Phase: N/A
Study type: Observational [Patient Registry]

The current guideline of asymptomatic severe hypertension (ASH) treatment in emergency department (ED) recommends through low level of evidence that the patients should not be rapidly decreased their BP in ED but instead receive oral antihypertensive treatment and close outpatient follow-up is needed. Unfortunately, there was some ambiguity in the time point of BP measurement in ED described in the past literature because high BP on ED admission may significantly decrease within hours without any medications. The importance of pre-ED discharge BP, which can still be critically high, that may affect the follow-up outcome has never been investigated. The study aim of this study is to evaluate the physicians' treatment strategies as well as immediate clinical outcomes between patients with severely- and moderately-elevated pre-discharge BP after management of ASH its in ED during the recent recommendation. The secondary outcome is to compare the BP at follow-up in these two groups.

NCT ID: NCT02533856 Completed - Patient Discharge Clinical Trials

Trial of Emergency Department Discharge With Enhanced Transitions of Care Compared to Usual Care

ETOC
Start date: August 2015
Phase: N/A
Study type: Interventional

This is a randomized controlled trial to assess the relative effectiveness of providing Enhanced Transitions of Care (ETOC) to improve patient outcomes after discharge from the Emergency Department (ED). Patients who are being discharged from the ED and have had a previous ED visit or hospital admission within the Thomas Jefferson Hospital System (TJUH or Methodist) within the past 90 days will be eligible for enrollment in this trial. Patients who consent to enrollment will be randomized to discharge by usual care or discharge with ETOC as provided by the company BoardRounds.

NCT ID: NCT02532387 Completed - Pulmonary Embolism Clinical Trials

Outpatient Treatment of PE and DVT in the Emergency Department

Start date: August 2015
Phase:
Study type: Observational [Patient Registry]

Standardize the approach to outpatient Pulmonary Embolism (PE) and Deep Vein Thrombosis (DVT) treatment.

NCT ID: NCT02531594 Completed - Smoking Cessation Clinical Trials

An Intervention to Reduce Second Hand Smoke Exposure Among Pediatric Emergency Patients

Start date: April 6, 2016
Phase: N/A
Study type: Interventional

This study will test the efficacy of a cessation intervention for caregivers in a large, inner-city Pediatric Emergency Department. The investigators will randomize 750 caregivers who smoke who present to our Pediatric Emergency Department with their child who has a Second Hand Smoke exposure-related illness to either one of two conditions: 1) Screening, Brief Intervention, and Assisted Referral to Treatment (SBIRT); or 2) Healthy Habits Control (HHC). The Screening, Brief Intervention, and Assisted Referral to Treatment condition will include a brief form of the Clinical Practice Guideline: Treating Tobacco Use and Dependence, motivational interviewing, engaging and personalized materials on the effects of smoking and Second Hand Smoke exposure, immediate access to caregivers' choice of cessation resources (e.g., Quitline, smokefree.gov, or txt2quit), a 12-week supply of nicotine replacement therapy and weekly booster materials for 12 weeks. The Healthy Habits Control program will be used as an attention control in which caregivers will receive instruction on healthy lifestyle choices to improve the child's health.

NCT ID: NCT02520661 Completed - Aging Clinical Trials

Paramedic Coached ED Care Transitions to Help Older Adults Maintain Their Health

Start date: February 3, 2016
Phase: N/A
Study type: Interventional

The emergency department (ED) is a common source of acute illness care for older adults. Many older adults who are discharged home from the ED return within 30 days due to numerous challenges faced during the ED-to-home transition. Unless programs to improve the ED-to-home transition are identified, the health and financial costs will only increase as the older adult population doubles by 2040. This study will apply Coleman's Care Transitions Intervention to the ED-to-home transition by adapting the program to account for the unique aspects of the ED setting. The research will evaluate the process, ED use, and cost outcomes of a community-based, paramedic-coordinated Care Transitions Intervention. Upon completion, this study will provide empiric evidence regarding this innovative approach to help the rapidly growing older adult population remain healthy and independent after an ED visit.

NCT ID: NCT02518919 Completed - Conscious Sedation Clinical Trials

Procedural Sedation And Analgesia in Children in the Emergency Department: The Role of Adjunct Therapies

Start date: October 1, 2015
Phase: N/A
Study type: Interventional

The role of Adjunct therapies such as Child Life therapy and Music listening during Procedural Sedation and Analgesia(PSA) for children during painful procedures has not been studied in the Emergency Department (ED). The investigators hypothesize that there will be a reduction in sedation medication dosage without change in sedation efficacy by addition of music therapy and Child Life to standard sedation protocol in children 3-15 years of age who undergo PSA for painful (orthopedic procedures, laceration repair, incision and drainage) procedures in a Pediatric emergency Department (PED).

NCT ID: NCT02518386 Completed - Suicide Attempts Clinical Trials

Epidemiology of Acute Self-poisoning in Emergency Services in France

EpiTox
Start date: March 2015
Phase:
Study type: Observational [Patient Registry]

Acute self poisoning is a leading cause of suicide attempts and leads to frequent emergency department visits. However, the exact epidemiology of acute self poisoning is not known. The description of the clinical pathway and the characteristics of patients with acute self poisoning could lead to an improvement in emergency care. The Investigators will conduct a 48h observational study in emergency services in France. Investigators primary objective is to gathered epidemiological clinical and treatment data during emergency dispatch, prehospital care and inhospital emergency care.

NCT ID: NCT02517463 Completed - Contraception Clinical Trials

Ulipristal Emergency Contraception Used Before or After Ovulation

Start date: May 2011
Phase:
Study type: Observational

This was a prospective, open-label, single-drug, uncontrolled, observational clinical study. Women attending the Family Planning Association of Hong Kong (FPAHK) for emergency contraception within 120 hours of UPSI were recruited. Subjects were recruited from both the Birth Control Clinics and Youth Health Care Centres of the FPAHK. Depending on the timing in relation to ovulation in the current menstrual cycle at the time of presentation, the women were classified into two groups: Group 1: pre-ovulatory Group 2: post-ovulatory After counseling and obtaining informed consent, eligible subjects received a single dose of ulipristal acetate 30 mg (ellaOne®) under direct supervision. A baseline blood test for hormonal profile (LH, oestradiol and progesterone) and ultrasound scan for ovarian follicle assessment were carried out by a designated doctor or research nurse at the clinic visit. The subjects were advised not to have further acts of coitus before the return of menstruation. They were given a diary chart to record vaginal spotting and bleeding, possible side effects and further acts of intercourse, if any, and the contraceptive method used. A follow-up appointment were be arranged about 1-2 weeks after the expected next menstruation. Any events of unplanned pregnancy and adverse effects were recorded for analysis.

NCT ID: NCT02512991 Completed - Clinical trials for ST-elevation Myocardial Infarction

Follow-up of Patients Bound for PCI After Implementation of a Helicopter Emergency Medical System

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

This study compares patients bound for Percutaneous Coronary Intervention (PCI) who were transported by either ground ambulance or emergency medical helicopter. The investigators describe long-term follow-up in relation to mortality and labour affiliation.

NCT ID: NCT02506478 Completed - Clinical trials for All Eligible ED Patients (Not Limited to a Particular Condition)

Juice Preference in the Emergency Department

JUICED
Start date: May 2015
Phase: N/A
Study type: Observational

ED patients who are able to drink juice will be approached and asked their beverage preference.