Clinical trial Recruiting at 1 site Observational Ages 18 to 100

One-stop photon-counting CT for patients after PCI

Official title: Diagnostic Performance and Prognostic Value of Multiparametric Photon-Counting Cardiac CT in Patients With Prior Coronary Stent Implantation: A Prospective Cohort Study

Run by Chinese PLA General Hospital · NCT07763340 · Data updated 2026-11-12

This study tests a single CT exam using photon-counting technology to image the heart after stent placement in people who have had PCI.

Quick facts

Study typeObservational
Ages18 Years to 100 Years
SexAll
Enrollment800 (estimated)
SponsorChinese PLA General Hospital
Academic / other
Drugs / interventionsradiation
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedJanuary 7, 2026
Main results expectedJanuary 7, 2029
Study endsJanuary 7, 2029
Registry record updatedAugust 13, 2026
Trial IDNCT07763340 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) who have a history of PCI with at least one coronary stent and can undergo iodinated CT with consent.

Probably not a fit

Patients who cannot receive iodinated contrast, have very poor renal function beyond institutional thresholds, or cannot comply with imaging procedures may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective observational cohort study aims to develop and validate a one-stop photon-counting CT imaging framework that can assess coronary anatomy, myocardial iodine distribution, extracellular volume, and cardiac function from one exam. The protocol may include ultra-high-resolution coronary CT angiography, resting myocardial iodine maps, delayed extracellular volume measurements, and a dose-controlled cine component. By reducing the need for multiple tests, the study seeks to streamline follow-up after PCI while limiting contrast exposure and radiation. The study is conducted at Chinese PLA General Hospital with adults who have at least one implanted stent.

Why it matters

Potential benefit: If successful, patients could benefit from a streamlined imaging approach that reduces the number of visits, contrast agents, and radiation exposure while providing comprehensive cardiac assessment after PCI.

How similar studies have gone: Previous imaging studies have explored photon-counting CT for cardiac imaging, but a fully integrated single-exam approach after PCI is innovative and continuously evolving.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age 18 years or older;
2. History of percutaneous coronary intervention with implantation of at least one coronary stent;
3. Ability to undergo iodinated contrast-enhanced CT;
4. Ability and willingness to provide written informed consent.

Exclusion Criteria:

1. Estimated glomerular filtration rate below the institutional threshold for contrast-enhanced CT, generally less than 30 mL/min/1.73 m², unless examination is clinically justified and approved according to institutional policy;
2. Known severe hypersensitivity to iodinated contrast material that cannot be adequately managed using the institutional premedication protocol; Pregnancy or suspected pregnancy;
3. Inability to provide informed consent or comply with study procedures;
4. Severe respiratory inability to perform the required breath-hold.

Where it's running

  • Chinese PLA General Hospital
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.