JPRN-jRCT1032200111招募中2 期
Safety and efficacy of transjugular biopsy using the AcquireTM Endoscopic Ultrasound Fine Needle Biopsy Device
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- Kato Naoya
- 入组人数
- 12
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
- >= 20age old 至 ot applicable（—）
- 性别
- All
入选标准
- •1) Patients who scheduled for a transvenous liver biopsy or transvenous renal biopsy due to chronic liver disease with/without renal impairment
- •2) Child-Pugh score A or B
- •3) Age is 20 years or older (any gender)
- •4) Patients who have been fully informed of and have obtained the written consent of their own free will to participate in the study.
排除标准
- •1) The patient who has one of the following cardiac diseases
- •a) Heart failure of NYHA class 3 or higher.
- •b) Current symptomatic coronary artery disease or a history of myocardial infarction within 4 weeks prior to enrollment.
- •2) Serious and active infection (CTCAE version 4.0 Grade 3 or higher)
- •3) Pregnant or lactating women and those who may or will become pregnant (if pregnancy is suspected, a pregnancy test should be performed).
- •4) There is a possibility of compromising patient safety or difficulty in complying with the study protocol.
研究者
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