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Improvement Image Quality for SuperSonic® MACH Ultrasound System (MACH IQ)

S

Supersonic Imagine

Status

Terminated

Conditions

Diagnosis

Treatments

Device: SuperSonic® Ultrasound System

Study type

Interventional

Funder types

Industry

Identifiers

NCT06360926
2024-A00526-41

Details and patient eligibility

About

The aim of this Study is to collect radiologist feedback to support the further development and improvement of the imaging modes implemented on the embedded software in the SuperSonic® Ultrasound System (including the probe).

Enrollment

55 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subject is ≥ 18 years old and is able to understand and sign the informed consent form.
  • Subject is a minor < 18 years old and the legal representative has signed the informed consent form.
  • Subject is scheduled for at least one or more routine ultrasounds.
  • Subject is affiliated to National Social Insurance or a Health Insurance Regimen.

Exclusion criteria

  • Subject is unable or unwilling to adhere to Study procedures.
  • Subject or his/her legal representative if a minor is unable to express or understand informed consent.
  • Subject is under legal protection
  • Subject is deprived of liberty by judicial or administrative decision
  • Subject undergoes psychiatric treatment under constraint
  • Subject is admitted to a health or social establishment for purposes other than research
  • Subject has latex allergy.
  • Subject has an open wound, cut, and/or a rash which would preclude an ultrasound imaging procedure

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

55 participants in 1 patient group

SuperSonic® Ultrasound System equipped with new software iterations used with a new probe
Experimental group
Treatment:
Device: SuperSonic® Ultrasound System

Trial contacts and locations

1

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Central trial contact

Ludovic HUET

Data sourced from clinicaltrials.gov

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