跳至主要内容
临床试验/NCT07058402
NCT07058402招募中不适用

A Multicenter, Randomized Controlled Trial Comparing the Retrograde Intrarenal Surgery With a Tip-Flexible Suction Access Sheath to the Standard Percutaneous Nephrolithotomy for the Treatment of 2-3 cm Unilateral Renal Stones

Changhai Hospital1 个研究点 分布在 1 个国家目标入组 308 人开始时间: 2025年4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
招募中
入组人数
308
试验地点
1
主要终点
Stone-Free Rate (SFR)

研究概览

简要总结

This is a multicenter, randomized controlled trial comparing retrograde intrarenal surgery (RIRS) using a tip-flexible suction access sheath with standard percutaneous nephrolithotomy (PCNL) for the treatment of 2-3 cm unilateral renal stones. The aim is to evaluate the clinical efficacy and safety of the novel suction sheath-assisted RIRS compared to standard PCNL in terms of stone-free rate and postoperative complications. A total of 308 patients will be enrolled across four centers in China.

详细描述

Kidney stones (renal calculi) are a common urological condition that can lead to pain, infection, and renal dysfunction. For renal stones measuring 2-3 cm, both retrograde intrarenal surgery (RIRS) and percutaneous nephrolithotomy (PCNL) are recognized treatment options. Traditional RIRS is less invasive but may be associated with lower stone-free rates for larger stones. A newly developed tip-flexible suction access sheath (TFS-UAS) allows improved access to renal calyces, reduces intrarenal pressure, and enables efficient stone fragment evacuation through continuous suction.

This study is a prospective, multicenter, randomized controlled trial designed to compare the effectiveness and safety of RIRS using the TFS-UAS versus standard PCNL in patients with unilateral renal stones measuring 2-3 cm. A total of 308 patients aged 18-80 years will be enrolled from four tertiary hospitals in China. Eligible participants will be randomized into two groups to receive either TFS-UAS-assisted RIRS or standard PCNL. The primary endpoint is the stone-free rate (SFR) at 3 months, assessed by CT scan. Secondary outcomes include postoperative infection rates, changes in hemoglobin and procalcitonin levels, hospital stay duration, and pain scores.

This study aims to provide high-quality evidence to guide surgical decision-making in the management of medium-sized kidney stones and to evaluate the potential advantages of the new suction-assisted sheath in minimally invasive endourology.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age between 18 and 80 years
  • •American Society of Anesthesiologists (ASA) physical status classification of I-III
  • •Single renal stone with a diameter between 2-3 cm confirmed by non-contrast CT scan
  • •Signed written informed consent and willingness to comply with study procedures

排除标准

  • •Anatomical abnormalities of the urinary tract (e.g., horseshoe kidney, ileal conduit)
  • •Uncontrolled urinary tract infection
  • •Absolute contraindications for RIRS or PCNL
  • •Inability to understand or complete study documentation
  • •Failure to follow study protocol or attend follow-up
  • •Patients requiring urgent rescue or at high risk for irreversible harm during surgery
  • •Patients who voluntarily withdraw from the study

研究组 & 干预措施

Retrograde Intrarenal Surgery (RIRS) with Tip-Flexible Suction Access Sheath

Experimental

Participants in this group will undergo retrograde intrarenal surgery (RIRS) using a tip-flexible suction access sheath for the treatment of 2-3 cm unilateral renal stones.

干预措施: Retrograde Intrarenal Surgery (RIRS) with Tip-Flexible Suction Access Sheath (Procedure)

Standard Percutaneous Nephrolithotomy (PCNL)

Experimental

Participants in this group will undergo standard percutaneous nephrolithotomy (PCNL) for the treatment of 2-3 cm unilateral renal stones.

干预措施: Standard Percutaneous Nephrolithotomy (PCNL) (Procedure)

结局指标

主要结局

Stone-Free Rate (SFR)

时间窗: 3 months postoperatively

The proportion of participants who are stone-free after the procedure, defined as no residual stones or residual fragments \<2 mm based on postoperative plain abdominal X-ray or non-contrast CT scan.

次要结局

  • Incidence of Postoperative Infection (SIRS Criteria)(Within 72 hours postoperatively)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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