DRKS00012565已完成未知
Comparison of a full-core end-cut biopsy device with a side-notch device: diagnostic valence of the specimen
niversitätsklinikum Regensburg0 个研究点目标入组 30 人开始时间: 2017年6月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 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
- 分配方式
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Patients undergoing clinically indicated biopsy of unclear liver lesions. Male patients and non-pregnant, non-lactating females aged =18 years of age, INR>1.4, thrombocyte count >10×109/l, informed consent signed.
排除标准
- •Any condition which, in the judgment of the clinical investigator or his designee, might increase the risk to the subject or decrease the chance of obtaining satisfactory data to achieve the objectives of the study. A mental condition rendering the patient unable to provide informed consent.
研究者
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