NCT07166471招募中不适用
Global Reference Ranges - Singapore
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- Perspectum
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- To determine the reference values for liver fibroinflammation in healthy adults from different ethnic groups.
研究概览
简要总结
We aim to undertake the Global Reference Range Study (GRR) to establish a set of healthy adult reference values for measures of fibroinflammation, fat and size/volumes for the liver, and other abdominal and thoracic organs to assess, compare, and if necessary, propose ethnicity specific reference ranges for these measurements.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female at least 18 years of age
- •Self-reported healthy
- •Willing and able to give informed consent for participation in the study
- •Willing and able to undergo an MRI
排除标准
- •History of cardiovascular disease as follows:
- •Myocardial infarction
- •Heart failure
- •Cardiomyopathy
- •Hospital admission/discharge for unstable angina
- •Heart surgery
- •Unstable angina
- •Transient ischemic attack
- •Presence of CVD risk factors such as hypertension, hyperlipidaemia, Type 2 diabetes, BMI > 30 kg/m2, smoker (current/ex-smoker)
- •History of non-cardiac diseases related to the lungs, liver, kidneys, pancreas or spleen judged by the study investigator as therefore unsuitable to participate in the study
- •The participant may not enter the study if they have any contraindication to magnetic resonance imaging (standard MRI exclusion criteria including pregnancy, extensive tattoos, pacemaker, shrapnel injury, severe claustrophobia)
- •Any other cause, including a significant disease or disorder which, in the opinion of the investigator, may either put the participant at risk because of participation in the study, or may influence the participant's ability to participate in the study
结局指标
主要结局
To determine the reference values for liver fibroinflammation in healthy adults from different ethnic groups.
时间窗: 24 months
次要结局
未报告次要终点
研究者
研究点 (1)
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