Actively Recruiting
Clinical Feasibility and Evaluation of Silicon Photon Counting CT
Led by GE Healthcare · Updated on 2025-11-06
100
Participants Needed
1
Research Sites
142 weeks
Total Duration
On this page
Sponsors
G
GE Healthcare
Lead Sponsor
S
Stanford University
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of the study is to collect data to evaluate utility of the using photon-counting CT in a clinical setting.
CONDITIONS
Official Title
Clinical Feasibility and Evaluation of Silicon Photon Counting CT
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years of age or older
- Able to sign and date the informed consent form
- Have had a clinically indicated CT exam of the head, neck, heart, chest, abdomen, pelvis, or extremities within the past 120 days or will have one within the next 30 days with images available
You will not qualify if you...
- Pregnant or lactating individuals
- Previously enrolled in this study
- Known or suspected allergy to iodinated contrast agents for contrast-enhanced CT exams
- Known or suspected renal insufficiency for contrast-enhanced CT exams as determined by site medical personnel
- Need for urgent or emergent care
- Any condition that might interfere with evaluation or pose a health risk as judged by the principal investigator or designee
- Unwilling to have GEHC personnel present during the CT exam
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Stanford University
Palo Alto, California, United States, 94304
Actively Recruiting
Research Team
M
Melissa Challman
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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