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NCT07133984Recruiting

STICH3C Cardiac Magnetic Resonance Observational Study

STICH3C Cardiac Magnetic Resonance (CMR) Observational Study (STICOS)

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

STICOS will test the hypothesis that residual jeopardized myocardium, late gadolinium enhancement, and non-ischemic substrate after revascularization is associated with postoperative adverse cardiovascular events such as heart failure , readmission, or death. This study will look at whether certain heart tissue abnormalities seen on MRI scans can help predict serious health problems after heart procedures like stents or bypass surgery.

Status (registry)
Recruiting
Study type
Observational
Enrollment
230 (estimated)
First submitted
14 Aug 2025
Start date
1 Mar 2024
Primary completion date
Aug 2028
Lead sponsor
Weill Medical College of Cornell University
NCT number
NCT07133984

What you commit to

  • Study type: Observational
  • Planned participants: 230
  • From 1 Mar 2024 to the primary completion date, Aug 2028
  • 10 sites in 6 countries
  • 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

  • Concomitant valve disease or other condition (e.g., LV aneurysm) requiring surgical repair or replacement

Other

  • Contraindication to CMR (i.e. magnetically activated materials), gadolinium, regadenoson/adenosine/dipyridamole
  • Active neoplasm and/or severe end-organ dysfunction with expected life expectancy less than 5 years.
    • \-

Who the study is looking for

  • Men and women ≥ 18 years old
  • LVEF ≤ 40% (quantified by echo, single-photon emission computed tomography \[SPECT\], or CMR within 2 months of enrollment)
  • Prognostically important CAD: either multivessel CAD (triple vessel or double vessel CAD including left anterior descendant artery (LAD), significant coronary stenosis defined as ≥ 70% based on coronary angiography, fractional flow reserve (FFR) ≤ 0.80 or instantaneous wave-free ratio (iFR) ≤ 0.89) or left main disease (+/- other CAD) for which significant stenosis defined as \> 50% based on coronary angiography, intravascular ultrasound (IVUS) minimum luminal area \[MLA\] value ≤ 6.0 mm2 (\< 4.5 mm2 Asian descent), or equivalent optical coherence tomography (OCT) measurements.
  • Either planned CABG/PCI within 3 months or CABG/PCI within the last 9 months.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
MU Vienna Austria
Coordinator of this site? Confirm its status
ViennaAustriaRecruiting
Libin Cardiovascular Institute
Coordinator of this site? Confirm its status
CalgaryCanadaRecruiting
Universite Laval Quebec (CRIUCPQ) Canada
Coordinator of this site? Confirm its status
QuébecCanadaRecruiting
Sunnybrook Health Sciences Centre
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting
Zbigniew Religa Lower Silesian Heart Disease Centre - Medinet
Coordinator of this site? Confirm its status
WroclawPolandRecruiting
Dedinje Cardiovascular Institute
Coordinator of this site? Confirm its status
BelgradeSerbiaRecruiting
NewYork-Presbyterian Brooklyn Methodist Hospital
Coordinator of this site? Confirm its status
BrooklynUnited StatesRecruiting
New York Presbyterian Queens
Coordinator of this site? Confirm its status
FlushingUnited StatesRecruiting
Weill Cornell Medicine/NewYork-Presbyterian Hospital
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.