JPRN-jRCT2051220042招募中2 期
A Single-Center, Randomised, Controlled Trial of the Efficacy and Safety of Inhaled Nitric Oxide therapy in the patients with severe right heart failure due to pulmonary hypertension
Ogo Takeshi0 个研究点目标入组 30 人开始时间: 2022年6月9日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 18age old 至 ot applicable(—)
- 性别
- All
入选标准
- •1) Patients who are at least 18 years of age at the time consent is obtained
- •2) Patients with pulmonary arterial hypertension (PAH) or chronic thromboembolic pulmonary hypertension (CTEPH)
- •3) Patients who meet all of the following criteria for right heart catheterization
- •1) Mean pulmonary artery pressure greater than 25 mmHg
- •2) Pulmonary capillary wedge pressure or left ventricular end-diastolic pressure less than 15 mmHg
- •3) Pulmonary vascular resistance greater than 3 Wood units
- •4) WHO-FC III or higher
- •5) Patients with fluid retention (fluid retention on physical examination or echocardiographic evidence of congestion), low cardiac output (cardiac coefficient less than 2.5 L/min/m2 ), or in need of inotropic drugs
- •6) Patients with written consent from the patient
排除标准
- •1) Patients with cardiac disease (Eisenmenger's syndrome) who are completely dependent on a right-left shunt for life support
- •2) Patients with PAH who are eligible for Calcium channel blockers
- •3) Patients with pulmonary veno-occlusive disease
- •4) Patients with pulmonary capillary haemangiomatosis
- •5) Patients with pulmonary hypertension due to left heart disease
- •6) Patients with pulmonary hypertension due to pulmonary disease and/or hypoxia
- •7) Patients with pulmonary hypertension with un clear and/or multifactorial mechanisms
- •8) Patients with a history of hypersensitivity to the investigational drug
- •9) Pregnant or lactating women, or patients who cannot consent to contraception during the study
- •10) Patients who plan to participate in other clinical trials or interventional studies during the period of this study
- •11) Patients who are judged by the investigator or subinvestigator to be inappropriate to participate in this clinical trial for other reasons.
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