Contrast-enhanced Ultrasound Versus CT Scan for Kidney Stone Patient Management — CEUS  

Ultrasonography Clinical Trial

Official title: Contrast-enhanced Ultrasound Versus CT Scan for Kidney Stone Patient

Status Withdrawn

Clinical Trial Summary

This study will be a randomized controlled study comparing the use of two clinical management strategies in nephrostomy tube management following percutaneous nephrolithotomy (PCNL). The first strategy entails using contrast-enhanced ultrasound (CEUS) to evaluate the renal collecting system (1). This is a new imaging approach applying ultrasound machines with special software in combination with intraluminal ultrasound contrast agent (Lumason) injection, which is an FDA-approved ultrasound contrast agent (2). The second strategy is a nephrostomy tube capping trial combined with low dose non-contrast computed tomography (CT) scan, one of the most frequently utilized clinical management strategies currently used in clinical practice (3).

Clinical Trial Description

This is a multi-center, randomized controlled study comparing the use of CEUS to CT scan plus capping trial immediately following PCNL. A total recruitment target of 1,046 subjects is planned and participants will be randomized into one of the two study arms. 1. Contrast-enhanced ultrasound (CEUS) arm: On postoperative day 1 (unless not clinically indicated), each subject will undergo CEUS with an administration of Lumason via their pre-placed nephrostomy tube. 2. Non-contrast CT scan plus capping trial arm: On postoperative day 1 (unless not clinically indicated), subjects' pre-placed nephrostomy tube will be capped and they will undergo a low dose non-contrast abdominal CT scan. Subsequently, nephrostomy tubes will be managed based on the results from these studies by the treating surgeon. Screening data will be reviewed to determine subject eligibility. Subjects who meet all inclusion criteria and none of the exclusion criteria will be entered into the study. The following investigational regimen will be used only in the CEUS arm: Experimental Investigation: Lumason at a 2 mL single dose, repeatable once at the time of imaging as needed. Subjects will be exposed to the randomization schema for 1 day during which they will undergo one of the two diagnostic imaging pathways. After that imaging study is complete, clinical care will proceed as per norm. Clinical and imaging data will be prospectively collected from the time of initial presentation until 6 months after surgery. The total duration of the study is expected to be 5 years to reach target accrual. Therefore, the investigators anticipate that the total duration of this study will be 4 years and 6 months for patient recruitment with the final 6 months used for collecting follow up data. ;

Related Conditions & MeSH terms

• Kidney Calculi
• Nephrolithiasis
• Ultrasonography

• NCT number: NCT03058614
• Study type: Interventional
• Source: University of California, San Francisco
• Status: Withdrawn
• Phase: Phase 2
• Start date: June 30, 2017
• Completion date: May 2, 2022