Improving ultrasound image quality with SuperSonic® MACH system
Improvement Image Quality for SuperSonic® MACH Ultrasound System
This study is trying to see if feedback from radiologists during routine ultrasound procedures can help improve the image quality of the SuperSonic® MACH Ultrasound System.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Sex | All |
| Sponsor | SuperSonic Imagine Industry-sponsored |
| Locations | 1 site (Paris, Ile De France) |
| Trial ID | NCT06360926 on ClinicalTrials.gov |
What this trial studies
This study aims to gather feedback from radiologists to enhance the imaging capabilities of the SuperSonic® MACH Ultrasound System. Participants will undergo routine ultrasound procedures, allowing researchers to assess and refine the system's embedded software and probe functionality. The focus is on collecting valuable insights that can lead to improved diagnostic imaging quality. By engaging healthcare professionals in this process, the study seeks to ensure that the ultrasound system meets clinical needs effectively.
Who should consider this trial
Good fit: Ideal candidates include adults and minors scheduled for routine ultrasound procedures who can provide informed consent.
Not a fit: Patients who are unable to adhere to study procedures or have conditions that preclude ultrasound imaging will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to enhanced ultrasound imaging quality, improving diagnostic accuracy for patients.
How similar studies have performed: While this approach focuses on feedback for system improvement, similar studies in ultrasound technology have shown potential for enhancing imaging quality.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Paris, Ile De France
- Hôpital Necker-Enfants malades — Paris, Ile De France, France (Recruiting)
Study contacts
- Study coordinator: Ludovic HUET
- Email: clinicals.ultrasound@supersonicimagine.com
- Phone: +336 83 93 03 79
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.