JPRN-jRCTs062180001已完成未知
CT-fluoroscopy-guided biopsy using a robot (Zerobot):single institution, single arm, open-label, prospective, feasibility trial - Robotic CT-guided biopsy
Hiraki Takao0 个研究点目标入组 10 人开始时间: 2018年8月31日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 10
研究概览
简要总结
Insertion of the biopsy introducer needle with our robot was feasible and safe at several locations in humans.
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) requirement for a pathologic diagnosis of a lesion in an extremity or the trunk (e.g., a lung, renal, liver, or soft tissue mass) using CT-guided biopsy
- •2) A platelet count >=30,000/mm3
- •3) An international normalized ratio <1.5
- •4) Age 20 years or older
- •5) Ability to provide written informed consent
- •6) A lesion >=10 mm in largest diameter
- •7) A scheduled needle tract <11 cm in length
排除标准
- •1) Limited mobility or impaired breath-holding ability
- •2) At-risk structures (e.g., the heart, great vessels, gastrointestinal tract, or pancreas) within 10 mm of the scheduled needle tract
- •3) Antiplatelet or anticoagulant therapy that cannot be withheld for the procedure
- •4) Inability to undergo anesthesia
- •5) A lesion located in the head and neck, central nervous system, spine, heart, great vessels, or gastrointestinal tract
- •6) A scheduled needle tract that passes through bone
- •7) Another biopsy for the lesion is scheduled
- •8) Invasive therapy, such as chemotherapy, radiation, and/or surgery, is scheduled to treat the lesion during the study period
- •9) Treatment for a psychiatric disorder
- •10) Pregnancy
- •11) Unsuitability for inclusion in the trial for whatever reason in the opinion of the investigators
研究者
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