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(3D) Ultrasound Imaging Liver and Kidney

W

Western University, Canada

Status

Enrolling

Conditions

Kidney Cancer
Liver Cancer

Treatments

Device: Ablation
Device: Biopsy

Study type

Observational

Funder types

Other

Identifiers

NCT03844399
6319 (Registry Identifier)

Details and patient eligibility

About

This study is to assess the addition of 3D ultrasound guidance during standard care ablation or biopsies of liver or kidney tumours. 3D ultrasound only differs from conventional 2D ultrasound in that the ultrasound transducer is mounted on a special assembly that moves the transducer in precise, stepped movements while a succession of 2D images are collected by the computer. Special software written specifically for 3D ultrasound precisely aligns these 2D images into a 3-demensional volume , allowing area in question to be viewed in many different planes. 3D ultrasound is a safe, fast, non-invasive imaging procedure. Ultrasound images will be checked against the pre- and post- procedure CT images to make sure the tumours were completely removed or properly targeted during biopsy.

Full description

Images will be acquired by a physician on patients who are undergoing a liver or kidney ablation or biopsy procedure who are well enough to provide consent. Patients will be imaged during the ablation procedure according to the standard of care, and subsequent analysis will commence following the acquisition. The devices being used are all property of the LHSC health network that have been licensed for clinical use through Health Canada. In addition, 3D ultrasound only differs from conventional 2D ultrasound in that the ultrasound transducer is mounted on a special assembly that moves the transducer in precise, stepped movements while a succession of 2D images are collected by the computer. Special software written specifically for 3D ultrasound precisely aligns these 2D images into a 3-dimensional volume, allowing the area in question to be viewed in different planes. The clinical 2D an d3D ultrasound images will be checked against the pre- and post- procedure CT images to make sure the tumours were completely removed.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Patients who are scheduled for standard care liver or kidney ablation or biopsy

Exclusion criteria

  • None

Trial design

40 participants in 1 patient group

Patients
Description:
Cancer patients who are scheduled to undergo an ablation or biopsy of a liver or kidney tumour
Treatment:
Device: Biopsy
Device: Ablation

Trial contacts and locations

1

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Central trial contact

Aaron Fenster

Data sourced from clinicaltrials.gov

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