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临床试验/NCT07272720
NCT07272720招募中不适用

Post-Market Clinical Follow-Up Investigation of MODULITH® SLX-F2 With StorM-Track in Patients With Kidney Stones - A Confirmatory Parallel-Group, Randomized Controlled Trial

Storz Medical AG2 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2025年12月11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
126
试验地点
2
主要终点
Stone-free rate (SFR)

研究概览

简要总结

Extracorporeal shockwave lithotripsy (ESWL) is a non-invasive standard treatment for kidney stones.

This study will be conducted to evaluate the effectiveness of ESWL using MODULITH® SLX-F2 with stone tracking, compared to MODULITH® SLX-F2 without stone tracking, in adult patients with kidney stones, as measured by stone-free status.

详细描述

The success of ESWL depends on multiple procedure- and patient-specific factors, one crucial factor being accurate stone targeting. Respiration induced kidney movement affects stone targeting as it results in the stone not being hit by the shock waves for up to 50% of the treatment time.

To improve the accuracy of stone targeting and comminution, an additional tracking module has been incorporated into the state-of-the-art lithotripter MODULITH® SLX-F2. The device is CE marked including its tracking module.

The scientific rationale for conducting this clinical investigation is based on the hypothesis that improved stone targeting through real-time tracking may lead to increased treatment efficacy and safety, as reflected by higher stone-free rates, reduced need for re-treatment, an increased quality of life, and lower adverse events rates.

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 (Outcomes Assessor)

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

  • Age ≥ 18 years
  • Single kidney stone (6 - 15 mm) in the target kidney
  • Stone density assessed by Hounsfield unit value (HU) ≤ 1,200 HU

排除标准

  • BMI > 34.9
  • Target stone that cannot be localised
  • Presence of one or more additional stones > 4 mm in the target kidney
  • Presence of one or more additional stones ≤ 4 mm located in the same calyx (upper, mid, or lower pole) or in the renal pelvis as the target stone
  • Stones with a density value of > 1,200 HU
  • Skin to stone distance (SSD) > 160 mm
  • The presence of obstructions, malformations or other factors preventing targeting or passing of the stone, including but not limited to the following:
  • Skeletal malformations and obesity, preventing targeting of the stone
  • Malignant tumour in the shockwave path
  • Arterial aneurysm or calcium deposits, or thrombosis in shockwave path
  • Brain, spinal column or air-filled tissue, especially the lungs, in the shockwave path
  • Obstruction distal to the stone (as this would hinder the passage of fragments through collecting system or ureter)
  • Any disease/medical condition, prior or concomitant medication/treatment/intervention, or implant that may affect this clinical investigation, and/or is contraindicated for the IMD, including but not limited to the following:
  • Severe nephrocalcinosis
  • Uncontrolled urinary tract infection
  • Coagulation disorders and bleeding diathesis, not compensated according to urological and hemostaseological guidelines
  • Anticoagulation or platelet inhibition therapy, not bridged according to urological and hemostaseological guidelines
  • Uncontrolled hypertension
  • Blood pressure > 180/100
  • Active cardiac implants that are not authorized for use with ESWL
  • Pancreatitis
  • Ehlers-Danlos syndrome
  • Administration of contrast agents containing gases for ultrasound diagnostics less than 24 hours before treatment.

研究组 & 干预措施

Standard ESWL without stone tracking (StorM-Track disabled).

Active Comparator

干预措施: Standard ESWL without stone tracking (StorM-Track disabled) (Device)

ESWL with kidney stone tracking (StorM-Track).

Experimental

干预措施: ESWL with kidney stone tracking (StorM-Track) (Device)

结局指标

主要结局

Stone-free rate (SFR)

时间窗: 6±2 weeks post 1st treatment

Proportion of subjects who are stone free or present with clinically insignificant residual fragments (measuring ≤ 4 mm on CT)

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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