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临床试验/NCT00206830
NCT00206830已完成2 期

SHORTness of Breath In the Emergency Department (SHORTIE)

Abbott RDx Cardiometabolic10 个研究点 分布在 1 个国家目标入组 306 人开始时间: 2005年4月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
306
试验地点
10
主要终点
Time to specific treatment for final diagnosis

研究概览

简要总结

SHORTIE is a two-phase study to determine the impact of the Triage Profiler S.O.B. (Shortness Of Breath) Panel on patient management, outcome, and cost.

详细描述

Patients presenting to the ED with a primary complaint of shortness of breath will a have blood sample collected at enrollment and tested using the Triage® Profiler S.O.B. Panel (measuring creatine kinase MB [CK-MB], myoglobin, troponin I, B-type natriuretic peptide [BNP], D-dimer). The test is used as an aid in the diagnosis of myocardial infarction (MI), an aid in the diagnosis and assessment of severity of heart failure (HF), and an aid in the assessment and evaluation of disseminated intravascular coagulation including pulmonary embolism (PE). Phase I is an observational study and results of the Triage Profiler S.O.B. panel will be blinded to all attending physicians and health care workers. In Phase II, patients will be assigned to either the experimental arm or the control arm of the study. In the experimental arm, the Triage Profiler S.O.B. Panel results will be available to the treating physician and can be incorporated into the decision making process. In the control arm, treating physicians and staff will be blinded to the Triage Profiler S.O.B. Panel results. Time to appropriate treatment, length of ED stay, patient outcome and hospital costs will be assessed in all patients and used to determine the impact of Triage Profiler S.O.B Panel on these parameters. Furthermore, the diagnostic accuracy of the Triage Profiler S.O.B Panel will be calculated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 and older.
  • Visit to the ED is due to a primary complaint of shortness of breath alone or shortness of breath with associated chest pain, cough or edema.

排除标准

  • Blood sample cannot be collected before treatment is initiated, specifically CPR or treatment with i.v. diuretics, injectable anticoagulants, thrombolytics
  • Patient is unwilling or unable to give consent to participate in the study
  • Patient has renal disease requiring dialysis
  • Patients with a clear exacerbation of isolated asthma
  • Patients with trauma that interferes with normal breathing function

结局指标

主要结局

Time to specific treatment for final diagnosis

Length of stay in the emergency department (ED)

ED and total hospital costs

次要结局

  • Outcome at 30 days (Phase I and II) and 90 days (Phase II)
  • Diagnostic accuracy of the Triage® Profiler S.O.B. panel for acute myocardial infarction (AMI), heart failure (HF) and pulmonary embolism (PE) in patients presenting with S.O.B.

研究者

发起方
Abbott RDx Cardiometabolic
申办方类型
Other

研究点 (10)

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