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Left Main Percutaneous Coronary Intervention Registry in Istanbul Medipol University Hospital

Comprehensive Registry of Left Main Coronary Artery Percutaneous Coronary Intervention Outcomes at Istanbul Medipol University Hospital

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06262971
Enrollment
3620
Registered
2024-02-16
Start date
2018-06-01
Completion date
2023-12-31
Last updated
2024-02-16

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

Conditions

Coronary Artery Disease, Left Main Coronary Artery Disease

Brief summary

This hospital-based registry study at Istanbul Medipol University Hospital focuses on documenting and analyzing the clinical and demographic characteristics, procedural-related aspects, and both short and long-term outcomes of patients undergoing left main coronary artery percutaneous coronary intervention (PCI). The study aims to identify predictors for adverse clinical outcomes in patients treated for left main coronary artery disease.

Interventions

DEVICEPercutaneous coronary intervention

balloon angioplasty, stent implantation, atherectomy, intravascular ultrasound.

Sponsors

Medipol University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* All patients undergoing any PCI procedure(s) in given timeframe will be included in this registry

Exclusion criteria

* Patients with no informed consent

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Major Adverse Cardiac Events (MACE) within One Year Following Left Main Coronary Artery PCIup to 1 month, 3 months, 1 yearThe primary outcome measure will be the incidence of major adverse cardiac events (MACE) within one year post-procedure in patients undergoing left main coronary artery PCI. MACE is defined as a composite of clinically significant endpoints including all-cause mortality, non-fatal myocardial infarction, non-fatal stroke, and any revascularization procedures required after the initial PCI.

Secondary

MeasureTime frameDescription
Ischemia-Driven Target Vessel Revascularization (ID-TVR) Ischemia-Driven Target Vessel Revascularization (ID-TVR)1 yearRevascularization procedure that is performed on a previously treated vessel in patients who have developed ischemia.
Procedure-Related Complications Within 30 Days of PCI1 monthThis outcome will document the incidence of procedure-related complications, including bleeding, vascular complications, or acute kidney injury, occurring within 30 days post-PCI.
Health-Related Quality of Life (HRQoL) Scores One Year After PCI1 yearHealth-related quality of life using standardized questionnaire (SF-36) one year after the PCI procedure
Rate of stent thrombosis1 month, 3 months, 1 yearProbable or definite stent thrombosis

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026