NCT07330622 Polish Registry of Percutaneous Coronary Intervention for Chronic Total Occlusions
| NCT ID | NCT07330622 |
| Status | Recruiting |
| Phase | — |
| Sponsor | National Institute of Cardiology, Warsaw, Poland |
| Condition | Coronary Occlusion |
| Study Type | OBSERVATIONAL |
| Enrollment | 1,000 participants |
| Start Date | 2025-05-21 |
| Primary Completion | 2026-05 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 1,000 participants in total. It began in 2025-05-21 with a primary completion date of 2026-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this observational study is to evaluate the safety, efficacy, and clinical outcomes of percutaneous coronary intervention (PCI) for chronic total occlusions (CTO) in patients treated in contemporary clinical practice in Poland. The main questions it aims to answer are: * What are the rates of procedural success and periprocedural complications of CTO PCI in routine clinical practice? * How do CTO PCI strategies and techniques, intravascular imaging, different treatment strategies, and mechanical circulatory support affect clinical outcomes? * How do clinical outcomes differ among different patient subgroups? * Can artificial intelligence-based analysis predict clinical and quality-of-life outcomes after CTO PCI? Patients undergoing CTO PCI as part of their standard medical care will be prospectively enrolled in a national, multicenter registry, with clinical, procedural, and follow-up data collected to evaluate real-world outcomes.
Eligibility Criteria
Inclusion Criteria: * Patients undergoing CTO PCI based on clinical grounds Exclusion Criteria: * Age \<18 years * Patient's refusal to participate in the registry
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07330622 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Coronary Occlusion. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07330622 currently recruiting?
Yes, NCT07330622 is actively recruiting participants. Contact the research team at mopolski@ikard.pl for enrollment information.
Where is the NCT07330622 trial being conducted?
This trial is being conducted at Bialystok, Poland, Grodzisk Mazowiecki, Poland, Inowrocław, Poland, Katowice, Poland and 11 additional locations.
Who is sponsoring the NCT07330622 clinical trial?
NCT07330622 is sponsored by National Institute of Cardiology, Warsaw, Poland. The trial plans to enroll 1,000 participants.