NCT06702917Active, not recruiting
GSI Cardiac on Revolution Apex - US
Wide Coverage GSI Cardiac Data Collection
Source: ClinicalTrials.gov · Last updated 15 Jul 2026
Brief summary (registry, in English)
The goal of this clinical data collection study is to collect raw CT scan data using a new GSI Cardiac mode on GE HealthCare's Revolution Apex CT system. Two groups of participants will be enrolled: A) Participants scheduled to undergo a Coronary CT Angiography (CCTA) as part of their standard of care B) Participants scheduled to undergo a cardiac catheterization or have a history of heart attack Participants in Group A will: -Have a standard of care CCTA immediately followed by a research GSI Cardiac scan Participants in Group B will: -Have a research CCTA immediately followed by a research GSI Cardiac scan Both groups will be in the study for approximately 1 day. There are no follow-up visits after the day of scan.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 50 (estimated)
- First submitted
- 22 Nov 2024
- Start date
- 10 Sept 2025
- Primary completion date
- 3 Apr 2026
- Lead sponsor
- GE Healthcare
- Diseases
- Coronary artery disease
- NCT number
- NCT06702917
What you commit to
- Study type: Observational
- Planned participants: 50
- From 10 Sept 2025 to the primary completion date, 3 Apr 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Who were previously enrolled in this study;
Other illness
- Anyone with known or suspected allergy to iodinated contrast agents;
- Anyone with known or suspected renal insufficiency as determined by site medical personnel;
- 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;
Other
- Subjects may be excluded from participating in study if they meet any of the following criteria:
- Who are pregnant or lactating;
- Who are in need of urgent or emergent care;
- Who are unwilling to have GEHC personnel present for the CT exam; AND,
- Cohort A: Undergoing a scheduled clinically indicated CCTA for anatomy assessment (aberrant origin, etc.)
Who the study is looking for
- Subjects may be included in this study if they meet the following criteria:
- Who are ≥18 years of age;
- Able to sign and date the informed consent form; AND,
- Cohort A: Undergoing a scheduled clinically indicated CCTA; OR,
- Cohort B: Known history of myocardial infarction or undergoing a clinically indicated cardiac catheterization due to known pathology.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Washington Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.