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Impact of Periodontal Treatment on Clinical Outcomes in Patients with Coronary Artery Disease Undergoing Percutaneous Coronary Intervention

Impact of Periodontal Treatment on Clinical Outcomes in Patients with Coronary Artery Disease Undergoing Percutaneous Coronary Intervention: A Prospective Study (PERIO-PCI) - PERIO-PCI

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000051921
Enrollment
300
Registered
2023-09-01
Start date
2023-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Coronary artery disease

Interventions

None listed

Sponsors

Tokyo Medical and Dental University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The study will target patients over 20 years of age with coronary artery disease (CAD) who undergo percutaneous catheter intervention (PCI) and who give informed consent to participate in this study. CAD includes stable angina as well as acute coronary syndromes (ACS) which consist of ST-elevation myocardial infarction, non-ST-elevation myocardial infarction, and unstable angina.

Exclusion criteria

Exclusion criteria: 1) Currently undergoing treatment for periodontal disease (PD) 2) Patients with cardiogenic shock, or hemodynamically or electrically unstable acute coronary syndrome (ACS) 3) Positive for COVID-19 4) Currently pregnant or breastfeeding 5) Carrying infectious diseases such as hepatitis virus or HIV.

Design outcomes

Primary

MeasureTime frame
The composite endpoint that includes cardiovascular death, non-fatal myocardial infarction, target lesion revascularization, and non-target lesion revascularization at 24 months

Secondary

MeasureTime frame
Inflammatory markers at 12 months (high-sensitivity CRP, IL-6, TNF-alpha)

Countries

Japan

Contacts

Public ContactMakoto Araki

Tokyo Medical and Dental University Cardiology Division

maraki.cvm@tmd.ac.jp+81-3-3813-6111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026