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Data Collection for New Spectral CT Imaging Method

This study is collecting data on a new type of imaging machine called a research CT (computed tomography) scanner. The goal is to see how well this investigational Spectral CT Imaging scanner works in a real-world medical setting. You might be able to join if you are 18 or older, can sign a consent form, and have had or will have a regular CT scan of your neck, chest, abdomen, pelvis, or extremities at St. Luke's University Hospital Network within a specific timeframe. The study will be considered successful if enough high-quality research scans are collected to help evaluate the new device. The current status of this study is unclear.

Study design
This is an observational study aiming to enroll 50 participants. It is designed to collect data on a new imaging method.
What's involved
Participants will undergo one research CT scan on an investigational Spectral CT Imaging scanner. This scan will be matched to a prior or scheduled standard-of-care CT scan.
Compensation
Not stated in the trial record.
Follow-up
Data collection will continue through study completion, which is expected to be an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07661706

Data Collection of New Spectral CT Imaging Method

Recruiting
Not specifiedAges 18+Observational
GE Healthcare
~50 participants
Updated 2026-06-22 on ClinicalTrials.gov
What's tested:Research CT

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Evaluable Raw Research Scans
Measured over Through study completion, an average of 1 year

Conditions

Computed Tomography

Explore related trials

Patients Undergoing Diagnostic Imaging

Where it's being run

1 sites across 1 states
Pennsylvania1

Study leadership

  • Brian Thomsen · STUDY_DIRECTOR · GE Healthcare

Who to contact

Melissa Challman, MPH, CCRP
[email protected]
18582213007
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

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

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.

What this trial measures

  • Evaluable Raw Research ScansThrough study completion, an average of 1 year

    Number of participants who research scan is deemed evaluable (i.e., no issues with participant motion or contrast administration/timing)