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临床试验/NCT05952635
NCT05952635已完成不适用

Tip Bendable Suction Ureteral Access Sheath vs. Traditional Ureteral Access Sheath in Retrograde Intrarenal Stone Surgery (RIRS): Study Protocol of a Multicentre, Prospective, Single-blinded, Randomized Controlled Trial

The First Affiliated Hospital of Guangzhou Medical University1 个研究点 分布在 1 个国家目标入组 320 人开始时间: 2023年8月2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
320
试验地点
1
主要终点
Immediate stone-free rate

研究概览

简要总结

Nephrolithiasis is the most common chronic kidney condition and affecting approximately one in every 10-17 people in the world[1,2]. Flexible ureteroscopy (f-URS) has become one of the most common treatments for ureteral and renal stones with minimal complications. The development of ureteral access sheath (UAS) is a significant advance in flexible ureteroscopic management of urinary stones. The UAS has two major advantages: 1) facilitating multiple entries into the renal collecting system without causing recurrent trauma to the ureter and permit expeditious basketing of multiple stone fragments, 2) improving the irrigation with better fluid outflow, thereby reducing the renal pelvic pressure (RPP) and risk of infectious complications.

The tip bendable suction ureteral access sheath (S-UAS) is a novel UAS that has good flexibility and deformability at the tip, which can passively bend (bend >90°) with the bending of f-URS and can connect to a vacuum suction device. Preliminary study showed that S-UAS can follow f-URS to cross the UPJ and into the renal pelvis and calices. S-UAS close to the stone can achieve complete stone-free status in RIRS. However, further clinical studies and comparisons with available techniques are required. This prospective, single-blinded, single-center, randomized control trial will evaluate the stone free rates, operative time, postoperative complications following RIRS with S-UAS. To the best of our knowledge, this is the first study to compare the clinical benefits of RIRS with S-UAS and traditional UAS.

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
Single (Participant)

入排标准

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

入选标准

  • Adults aged ≥ 18 years;
  • American Society of Anesthesiology score 1-3;
  • Upper urinary stone (kidney stone or upper ureteral stone) diameter of ≤ 3 cm confirmed by CT;
  • Capable of giving written informed consent, which includes adherence with the requirements of the trial.

排除标准

  • Patients with abnormal urinary tract anatomy (such as horseshoe kidney or ileal conduit);
  • Patients with uncontrolled UTI;
  • Patients with health or other factors that are absolute contraindications to RIRS;
  • Patients unable to understand or complete trial documentation.

结局指标

主要结局

Immediate stone-free rate

时间窗: Postoperative day 1

No residual stone, or no stone fragments larger than 2 mm on KUB and ultrasound at postoperative day 1 are defined as stone free.

次要结局

  • Duration of hospital stay(From date of operation until the date of discharge, assessed up to 2 weeks.)
  • Complications up to 3 months post randomization(Postoperative 3 month)
  • Operative time(From start of operation until the end of operation, assessed up to 2 weeks.)
  • Stone-free rate at 3 months(Postoperative 3 month)
  • Further interventions received up to 3 months post randomization(Postoperative 3 month)
  • Change of Quality of life Score (prior to surgery and at month 3 after randomization)(Postoperative 3 month)

研究者

发起方
The First Affiliated Hospital of Guangzhou Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Guohua Zeng

Vice president

The First Affiliated Hospital of Guangzhou Medical University

研究点 (1)

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