PCI Registry at University Hospital Basel for Complex Coronary Procedures

Is this trial a fit for you?

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

What this trial studies

The PCI Registry Basel is an observational registry that gathers routine clinical data from adults undergoing PCI at University Hospital Basel. It aims to compare outcomes across treatment strategies, including DES, DCB, and BRS, across a spectrum of complex procedures such as CTOs and bifurcations. Data are retrospectively extracted from existing medical records and catheterization lab reports, with no extra interventions or visits required for participation. All information is pseudonymised before analysis, and a secure code link to identifiers is kept separate under control of the Principal Investigator. The study seeks to identify which strategies work best for different patient groups in routine clinical practice to inform future care.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Patients treated at the University Hospital Basel

* Undergoing complex PCI (e.g. left main, bifurcation, multivessel PCI, rotational atherectomy or other calcium modification, complex anatomy). The definition complex will be a clinical/ procedural/ anatomical definition made by the operator.
* Undergoing CTO or CHIP (Complex High-risk Indicated Patient) procedures
* Treated with a DCB strategy
* Treated with a BRS

Exclusion Criteria:

* Patients under 18 years of age

Where it's running

• University Hospital Basel
  Basel, Canton of Basel-City, Switzerland Recruiting

Study contacts

• Principal investigator: Gregor Leibundgut, Prof. Dr. med. — University Hospital, Basel, Switzerland
• Study coordinator: Gregor Leibundgut, Prof. Dr. med.
• Email: gregor.leibundgut@usb.ch
• Phone: (0)61 556 58 18

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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.