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临床试验/NCT05022537
NCT05022537撤回不适用

RetroPerc®-A Prospective, Multi-institutional Trial of Efficacy of the RetroPerc Device

The University of Texas Health Science Center, Houston1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
入组人数
50
试验地点
1
主要终点
Number of patients with symptom free survival as defined as lack of flank pain

研究概览

简要总结

The purpose of this study is to determine the efficacy of RetroPerc® in obtaining renal access for percutaneous nephrolithotomy

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Renal pelvis and proximal ureteral stones >10 mm confirmed with non-contrast computed tomography

排除标准

  • Suspected pyelonephritis.
  • Prior percutaneous nephrolithotomy procedure in affected kidney.
  • Mid-ureteral or distal ureteral stones.
  • Pregnancy.
  • Anatomical abnormal kidney, including:
  • Horseshoe

研究组 & 干预措施

Treatment (retrograde nephrostomy)

Experimental

干预措施: retrograde nephrostomy (Device)

Control Group ( antegrade nephrostomy)

Active Comparator

干预措施: antegrade nephrostomy (Device)

结局指标

主要结局

Number of patients with symptom free survival as defined as lack of flank pain

时间窗: 6-12 weeks after procedure

Number of patients with symptom free survival as defined as lack of limitations to social or daily activities.

时间窗: 6-12 weeks after procedure

Treatment efficacy as measured by total time of lithotomy operation fluoroscopy

时间窗: (end of procedure)about 3 hours after start of procedure

Treatment efficacy as measured by the time taken from diagnosis to nephrostomy access

时间窗: end of procedure (about 4-8 weeks from diagnosis)

Treatment efficacy as measured by total time of access operation fluoroscopy

时间窗: end of procedure( about 90 minutes after start of procedure)

Treatment efficacy as measured by total time of lithotomy operation

时间窗: end of procedure(about 3 hours after start of procedure)

Treatment efficacy as measured by length of post-operative hospital stay

时间窗: 24 hours after procedure

Number of patients with symptom free survival as defined as lack of presence of urinary or gastrointestinal symptoms,

时间窗: 6-12 weeks after procedure

Number of patients with symptom free survival as defined as lack of limitations to work

时间窗: 6-12 weeks after procedure

Treatment efficacy as measured by total time of access operation.

时间窗: end of procedure( about 90 minutes after start of procedure)

Number of patients that are stone free

时间窗: 6-12 weeks after procedure

stone free is defined as \<2mm on non-contrast computed tomography

次要结局

  • Number of patients that require pain medication (defined as discharge with an opioid prescription).(6-12 weeks after procedure)
  • Number of patients with nephrostomy access adequate for stone treatment(end of procedure( abut 3 hours from start of procedure))
  • Number of patients with normal laboratory values(24 hours after procedure)
  • Number of patients with an infection rate which is defined as a positive culture within the study time period(6-12 weeks after procedure)
  • Number of patients with normal vital signs(end of procedure( abut 3 hours from start of procedure))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nadeem N Dhanani

Assistant Professor

The University of Texas Health Science Center, Houston

研究点 (1)

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