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Cardiac Stent Study: A prospective observational registry study.

Cone flare crush modified T stent bifurcation registry: A prospective observational registry study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12618001145291
Acronym
CFCT Study
Enrollment
20
Registered
2018-07-12
Start date
2018-04-11
Completion date
2019-03-20
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Patients undergoing bifurcation coronary stenting as part of standard of care and who give informed consent will be included in this study. All of the following are part of standard of care: Participants will be seen in pre-admission clinic or in their hospital bed by the PI. The registry will be discussed and if agreeable informed consent will be obtained. The participant will have a bifurcation stent inserted, discharged from hospital and followed up in the clinic at the Princess Alexandra Hospital. An exercise echocardiogram will be performed at Month 12 and if this is positive a coronary angiogram will be performed. The registry then ends for the participant. Registry research: Data from all of these time points will be collected.

Interventions

Standard of care bifurcation stenting will occur. Patients will be observed post-procedure for 12 months for any cardiovascular outcomes. Visits will occur at Discharge, 30 days, 6 months and 12 months. The participant will be reviewed by their cardiologist at each visit.

Sponsors

Princess Alexandra Hospital
Lead SponsorHospital

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

• Age equal to or greater than 18yrs • Planned two-stent bifurcation technique using a platinum chromium everolimus drug eluting stent with abluminal bioresorbable drug eluting polymer for a bifurcation stenosis where the side-branch is 2.5 mm or greater in diameter and the operator has determined a two stent CFCT technique is required • Non-emergent setting • ACS patients included if undergoing a staged procedure • Written informed consent.

Exclusion criteria

• Patients in whom the insertion of a bifurcation stent is not clinically indicated • Patients in whom the insertion of a bifurcation stent is not clinically advised (for example inability to take dual antiplatelet therapy because of bleeding diathesis). • Patients undergoing primary PCI for ST elevation myocardial infarction or rescue PCI for failed fibrinolysis • Women of childbearing potential with a positive pregnancy test.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 25, 2026