NL-OMON38739已完成不适用
Central Hemodynamics, Augmentation index and Microcirculation after Phlebotomy - CHAMP study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 42
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Without volume replacement:
- •- Patients aged 18-75 years receiving phlebotomy at regular intervals (for example because of hemochromatosis, porphyria and polycythemia vera)
- •- Known to tolerate phlebotomy
- •- Willing to participate
- •- Able to provide informed consent.
- •Patients which are known to tolerate phlebotomy without any adverse events are included in the *no-volume replacement group.* Patients who have experienced adverse events after phlebotomy in the past, and are previously assigned to receive volume replacement by their attending physician, are included in the *volume replacement group.* We aim to include the same amount of patients in each group.
排除标准
- •- Pacemaker or ICD device
- •- Atrial fibrillation
- •- Mechanical heart valve
- •- Congestive heart failure (*NYHA III/IV)
- •- Unable to stand up
- •- Uncontrolled hypertension (BP>180/110 mmHg)
研究者
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