ACTRN12614000630617进行中（未招募）未知
A single centre, randomised, unblinded, prospective trial on the diagnostic performance and cost of coronary computed tomographic angiography compared to exercise stress angiography in patients presenting to the emergency department with chest pain suspected of acute coronary syndrome.
Queensland Emergency Medicine Research Foundation0 个研究点目标入组 592 人开始时间: 2014年6月13日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 592
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Diagnosis
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 30 Years 至 85 Years（—）
- 性别
- All
入选标准
- •Males greater or equal to 30 and females greater or equal to 40 years of age presenting to the ED with acute undifferentiated chest pain were eligible for inclusion in the trial. Inclusion criteria included intermediate probability of coronary artery disease according to the Cardiac Society of Australia and New Zealand guidelines; initial 12-lead ECG without evidence of acute ischemia, TIMI (Thrombolysis in Myocardial Infarction) risk score <4 and a negative first serum sensitive troponin-I with a 99th centile at <0.04 ng/ml (Access 2 immunoassay, Beckman-Coulter)
排除标准
- •Exclusion criteria were previous diagnosis of coronary artery disease; confirmed pregnancy or lactating female; history of severe reactive airway disease or current exacerbation; allergy or contraindication to iodinated contrast or beta-blockade medications; current atrial fibrillation; renal impairment (eGFR < 50ml/minute using the MDRD equation). To be eligible for randomization, subjects needed to be pain-free and potentially able to exercise on a treadmill.
研究者
相似试验
尚未招募
Unknown
A single-centre study to check the visual performance and reduction in farsightedness in children with use of DIMSHYP spectacle lensesCTRI/2024/08/072260Dr. Agarwal’s Eye Hospital Limited
进行中（未招募）
不适用
A single centre, randomised, partially-blind, placebo-controlled 3 way crossover pilot study investigating efficacy in terms of heartburn relief after taking (2x250mg) Gaviscon® chewable tablets, (1x20mg) Losec® MUPS® tablet and (2x) Placebo tablets in subjects with heartburn following a refluxogenic meal. - Three-period crossover pilot study in healthy subjects susceptible to heartburn.Investigating efficacy in terms of heatburn relief in healthy subjects following a refluxogenic meal.EUCTR2010-019414-24-GBReckitt Benckiser Healthcare (UK) Ltd
招募中
不适用
Applying a high frequency stimulator intended for shoulder pain patientsKCT0002545Chonbuk National University Hospital38
进行中（未招募）
1 期
A single centre, randomised, single blind, parallel group single dose study to compare the speed of onset of ibuprofen gel, ibuprofen gel with levomenthol and diclofenac gel in the relief of pain from strains, sprains and sports injuriesPain of strains, sprains and sports injuriesMedDRA version: 18.1 Level: PT Classification code 10065016 Term: Post-traumatic pain System Organ Class: 10022117 - Injury, poisoning and procedural complicationsEUCTR2015-005240-33-GBThe Mentholatum Company Ltd182
已完成
不适用
A single centre, prospective, randomised, double-blind, placebo controlled, sequential, dose-escalating phase I study to assess the safety and tolerability of intravenously infused single doses of OPN-305 in healthy subjects.inflammatory reactionsrejections10038365NL-OMON38332Opsona Therapeutics Ltd.50