NCT06277895招募中不适用
Application of Emergency Rapid Detection of Expiratory Volatile Organic Compounds (VOCs) in Patients With Acute Cardiogenic Chest Pain
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 1,400
- 试验地点
- 1
- 主要终点
- Baseline VOCs (aldehydes) levels in healthy population
研究概览
简要总结
The goal of this observation study is to compare VOCs in cardiogenic chest pain population/health conditions, to answer：Establishment and promotion of the application system of emergency rapid detection of expiratory Volatile Organic Compounds (VOCs) in patients with acute cardiogenic chest pain
- VOCs levels were measured at baseline in healthy people, and markers of VOCs that could be used to identify acute cardiogenic chest pain were sought.
- The relationship between abnormal VOCs (mainly aldehydes) and prognosis of patients and the correlation with Super-score for early warning of acute heart failure.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Observation group inclusion criteria:
- •Over 18 years old, male or female;
- •Patients with acute cardiogenic chest pain (see diagnostic criteria);
- •Patient's informed consent.
- •Inclusion criteria of healthy control group:
- •Over 18 years old, male or female;
- •Centerless cerebrovascular disease, lung disease, no abnormal liver and kidney function, no acute infection recently;
- •Informed consent.
排除标准
- •The patient had difficulty in collecting breath;
- •Patients with terminal illness or receiving palliative care;
- •Have participated in other clinical studies or consider it inappropriate to participate in this study.
研究组 & 干预措施
normal group
Other
Healthy population
干预措施: VOCs (Diagnostic Test)
cardiogenic chest pain group
Experimental
cardiogenic chest pain group/acute coronary syndrome
干预措施: VOCs (Diagnostic Test)
结局指标
主要结局
Baseline VOCs (aldehydes) levels in healthy population
时间窗: Baseline
Baseline VOCs (aldehydes) levels in healthy population
次要结局
- MACE in patients with cardiogenic chest pain(From enrollment to the end of treatment at 30 days)
研究者
研究点 (1)
Loading locations...
相似试验
已完成
不适用
Efficacy Evaluation of Observation Unit Cardiac Magnetic Resonance Imaging (MRI) in Patients With Intermediate Risk Acute Chest PainChest PainAcute Coronary SyndromeNCT00869245Wake Forest University Health Sciences124
已完成
4 期
Providing Rapid Out of Hospital Acute Cardiovascular Treatment (PROACT)NSTEMINCT01634425University of Alberta601
终止
2 期
Cardiovascular Events From Trifluridine/Tipiracil +/- Oxaliplatin in Colorectal/Oesogastric Adenocarcinoma PatientsColorectal AdenocarcinomaOesogastricNCT04894123GERCOR - Multidisciplinary Oncology Cooperative Group1
已完成
不适用
Evaluation of Predictive Factors for Right Ventriculaire DysfunctionRight Ventriculaire DysfunctionNCT04596982Assistance Publique - Hôpitaux de Paris18
Unknown
不适用
Observatory on Emergency Care for Acute Coronary Syndrome in Grand Est of FranceAcute Coronary SyndromeNCT02887066Central Hospital, Nancy, France580