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临床试验/NCT04435132
NCT04435132已完成不适用

Robotic-assisted Percutaneous Access: Interventional, Non-randomized, Open-label, Non-comparative and First-in-Man Study

NDR Medical Technology Pte Ltd2 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2018年8月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
5
试验地点
2
主要终点
Needle insertion time

研究概览

简要总结

This is a first-in-man (FIM) study to show feasibility and safety profile of the newly developed robotic device for percutaneous access in PCNL surgery. Patients with renal stone disease who had standard indications for prone PCNL were included in the study. PCNL was conducted with percutaneous puncture with the aid of robotic device with the use of intra-operative fluoroscopy. 5 patients were recruited in this pilot study over a period of 3 months. Punctures were performed by the board-qualified urologist.

详细描述

All patients underwent preoperative investigations and imaging study (CT Urogram/Intravenous Pyelography) done prior to the operation as per standard operation preparation. Intraoperatively fluoroscopic imaging was done for the patients and the images were synchronized to the software. Robotic arm was placed on the site of surgery as for prone PCNL and diaphragm of the arm was centred over the site of desire calyx of entry. A needle was engaged into the centre of the diaphragm and using the software the need was aligned in the line of puncture automatically based on the fluoroscopic images. After the alignment was done the needle was advanced manually by the surgeon until the entry was confirmed by efflux of urine from the puncture needle. After the entry was confirmed a standard PCNL using 24 F or 30 F Balloon dilator was performed and stone cleared using Cyberwand/ Shockpulse etc. All the intraoperative and perioperative parameters as mentioned in the data collection form was measured. Results was analysed with the main focus on time of obtaining the puncture, accuracy of puncture, radiation exposure time till calyceal entry which was confirmed by free flow of urine and for any complications.

Patients aged between 21 to 75 years old who were diagnosed with kidney stone diseas and planned for prone PCNL with indication for surgery as per standard of care were recruited. They understood the purpose of testing and offered their voluntary and informed consent.

The robotic device i.e. ANT lesses the learning curve of percutaneous access as it reduces the need for surgeon's visualization of the calyceal system and the needle alignment. It also improved efficiency as there is less dependence on human skills during the procedure. As a whole, the FIM trial was a success. The performance of the ANT system during the trial was satisfactory. The robot alignment time is less than 30 seconds. Total puncture time was around 6 minutes and no AEs were reported.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Device Feasibility
盲法
None

盲法说明

Patients will undergo prone PCNL under fluoroscopic guidance and with the aid of the robotic device. They will then be admitted to inpatient ward as per standard of care for PCNL.

入排标准

年龄范围
21 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 21 to 75 years
  • Diagnosed with kidney stone disease and planned for prone PCNL with indication for surgery as per standard of care
  • Subject who understand the purpose of testing, voluntary and informed consent, patients undergoing invasive imaging follow-up.

排除标准

  • Bleeding disorders
  • Patient on anticoagulation/antiplatelets drugs
  • Pyonephrosis
  • Pregnant women
  • Not able to have prone position for the procedure due to comorbidities
  • Moderate to severe renal failure
  • The patient's life expectancy is less than 12 months
  • Poor compliance and patients unable to complete the study in accordance with the requirements.

结局指标

主要结局

Needle insertion time

时间窗: During procedure

Time taken for PCNL procedure

Needle alignment time

时间窗: During procedure

Time taken for needle alignment

Radiation dosage from placement of robot to efflux of urine

时间窗: During procedure

A measure of the radiation exposed during the surgical procedure

Time to target

时间窗: During procedure

Time taken for the needle to reach the calyx, from on the skin to successful needle targeting

Radiation dosage from placement of robot to successful needle target via image confirmation

时间窗: During procedure

A measure of the radiation exposed during the surgical procedure

Number of needle insertion attempts to obtain access

时间窗: During procedure

Number of attempts before successfully reaching the calyx

次要结局

未报告次要终点

研究者

发起方
NDR Medical Technology Pte Ltd
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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