Data Collection of New Spectral CT Imaging Method

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGE Healthcare

About this trial

The purpose of the study is to collect data to evaluate utility of a next generation spectral CT system in a clinical setting.

Eligibility criteria

Qualifiers

Who are ≥18 years of age;

Able to sign and date the informed consent form; AND,

Who have in the past 90 days or will in the future 30 days of the investigational scan undergo a clinically indicated CT exam within the St. Luke's University Hospital Network of the neck, chest, abdomen, pelvis, or extremities.

Disqualifiers

Who are pregnant or lactating;

Who were previously enrolled in this study;

For planned contrast-enhanced investigational CT exams, anyone with known or suspected allergy to iodinated contrast agents;

For planned contrast-enhanced investigational CT exams, anyone with known or suspected renal insufficiency as determined by site medical personnel;

Trial design

Treatments tested in this trial

  • Research CT

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators