Purpose

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

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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; - Who need urgent or emergent care; - Who have any conditions that, in the opinion of the PI or designee, would interfere with the evaluation of the results or constitute a health hazard for the subject; OR, - Who are unwilling to have GEHC personnel present for the CT exam.

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Other

Arm Groups

ArmDescriptionAssigned Intervention
Research CT
  • Device: Research CT
    Participants will undergo a research CT on an investigational Spectral CT Imaging scanner which will be matched to their prior or scheduled SOC CT. Scans will be matched on anatomy, radiation dose, and contrast administration.

Recruiting Locations

St Luke's University Health Network
Bethlehem, Pennsylvania 18015
Contact:
Monica Hosler
484-658-4567
monica.hosler@sluhn.org

More Details

Status
Recruiting
Sponsor
GE Healthcare

Study Contact

Melissa Challman, MPH, CCRP
18582213007
melissa.challman@gehealthcare.com

Detailed Description

Data collected in this study includes an assessment of image quality parameters to evaluate the product. This data and analysis will help support regulatory submissions.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.