Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07390994

The PICCOLETO IX PHENO Study

To investigate whether pre-procedural OCT-derived de novo coronary lesion phenotype (lipid-rich, fibrotic, calcific; and ACS mechanisms such as plaque rupture/erosion/calcified nodule) is associated with clinical outcomes after DCB angioplasty.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

About this study

PICCOLETO IX PHENO is an investigator-initiated, multicenter, international, ambispective (retrospective and prospective) cohort study enrolling patients who underwent DCB angioplasty for de novo coronary artery disease with preprocedural OCT assessment of the target segment. OCT images (baseline mandatory; post-preparation and post-PCI when available) and angiography will be analyzed by independent core laboratories; clinical events will be adjudicated by an independent committee. The primary endpoint is clinically-driven target lesion revascularization at 12 months; secondary endpoints include device-oriented composite endpoint (cardiac death, TLR, target-vessel MI), target vessel revascularization, MI endpoints, and mortality.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Chronic coronary syndrome or acute coronary syndrome diagnosis (per ESC guidelines).
  • De novo obstructive CAD: ≥50% left main stenosis, or any stenosis ≥70%, or FFR <0.80 in any other major epicardial vessel, or MLA deemed ischemic at intravascular imaging.
  • OCT assessment of the target segment phenotype prior to lesion preparation and DCB angioplasty.
  • Successful DCB angioplasty according to DCB ARC criteria.
  • Patients who underwent DCB-only PCI, or hybrid DCB-DES PCI with at least 20 mm of the target segment treated with DCB.

Exclusion criteria

  • Previous revascularization of the target segment with stent.
  • Hybrid DCB-DES PCI with DCB-treated segment <20 mm and/or lacking complete OCT assessment of the DCB-treated segment and/or bailout stenting.
  • Lack of at least 6 months of clinical follow up.
  • PCI of chronic total occlusion.

Treatment and study plan

Primary outcomes

  1. Clinically-driven Target Lesion Revascularization (TLR)

    Time frame: 12 months

    Any repeat revascularization (percutaneous or surgical) of the target lesion performed for recurrent symptoms or objective evidence of ischemia attributable to the target lesion.

Secondary outcomes

  1. Device-Oriented Composite Endpoint (DOCE)

    Time frame: 12 months

    Composite of cardiac death, target-vessel myocardial infarction, and clinically-driven target lesion revascularization.

  2. Target Vessel Revascularization (TVR)

    Time frame: 12 months

    Any repeat revascularization (percutaneous or surgical) of the target vessel.

  3. All-cause Mortality

    Time frame: 12 months

    Death from any cause during the study follow-up period.

  4. Cardiac Death

    Time frame: 12 months

    Death attributed to cardiovascular causes, including death from unknown cause.

  5. Target-Vessel Myocardial Infarction (TV-MI)

    Time frame: 12 months

    Myocardial infarction attributable to the target vessel based on clinical, electrocardiographic, and biomarker criteria according to the Fourth Universal Definition of Myocardial Infarction.

  6. Any Myocardial Infarction

    Time frame: 12 months

    Any myocardial infarction (target-vessel or non-target-vessel) according to the Fourth Universal Definition of Myocardial Infarction.

Study contacts

Contact information is provided by the study sponsor or research team.

Beatrice Barbano

CONTACT

Filippo Gurguglione

CONTACT

mailto:[email protected]

+393312048150

Sponsors and collaborators

Lead sponsor

Fondazione Ricerca e Innovazione Cardiovascolare ETS

Other

Registry information

Official study title

Prognostic Impact of PHENOtyping de Novo Coronary Artery Disease Prior to Drug-Coated Balloon Angioplasty by Optical Coherence Tomography (PICCOLETO IX PHENO)

Acronym: PIX-PHENO

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Feb 5, 2026
Registry last updated
Feb 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.