Which contrast agent gives clearer heart artery images?
NCT ID NCT05065073
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This trial compares two types of contrast agents used during optical coherence tomography (OCT), a test that takes detailed pictures of the heart's arteries. The study will see if one agent uses less contrast, produces clearer images, and causes fewer heart rhythm changes than the other. Adults with coronary artery disease who are already scheduled for OCT will be randomly assigned to receive either the iso-osmolar or low-osmolar contrast agent.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Iodixanol (iso-osmolar contrast) and Iohexol (low-osmolar contrast)
- What this could lead to
- If one contrast agent works better, it could make OCT imaging safer and more efficient for people with coronary artery disease.
- What could go wrong
- This is a small, single-center trial, so results may not apply broadly. The study focuses on imaging details, not long-term patient outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
62 people
The number who actually took part.
- Started
-
Sep 2021
- Finished
-
Jun 2023
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 18 years or greater 2. Willing and able to give informed consent. The patients must be able to comply with study procedures 3. Undergoing clinically-indicated coronary angiography and OCT Exclusion Criteria 1. Baseline electrocardiographic changes hindering interpretation (such as left bundle-branch block, and \>1 mm ST segment depression) 2. Emergency cardiac catheterization (for example in patients with ST-segment elevation acute myocardial infarction) 3. Inability to provide symptomatic assessment 4. Known allergy to contrast
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Minneapolis Heart Institute Foundation
Minneapolis, Minnesota, 55407, United States
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