A Study to Evaluate the GE Ultrasound System Performance

Overview

About this study

The purpose of this study is to evaluate the performance of the investigational GE Ultrasound Systems including image quality, under clinical conditions and to obtain feedback from experienced users.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Have a clinical indication for an ultrasound exam;
  • Are adults (aged 18 years or older) at the time of consent;
  • Are eligible to undergo ultrasound scanning per the site standard of care; AND
  • Are able and willing to provide written informed consent for participation.

Exclusion Criteria

Subjects who meet any of the following criteria will not be included:

  • Expected to be at increased risk due to study participation (e.g. due to allergies, sensitivities), in the medical opinion of an investigator;
  • Previously participated in this study, or are enrolled in another active GEHC study or other research study that could be expected to interfere with participation in study procedures, in the opinion of the investigator;
  • Require or are anticipated to require immediate medical care in which study participation may reasonably delay his/her medical care.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Nirvikar Dahiya, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

International patient clinical studies questions