Actively Recruiting

Age: 20Years +
All Genders
ID01889459

Patient Registry of Percutaneous Coronary Intervention (PCI) for Chronic Total Occlusion (CTO) by Japanese Experts

Led by Kurashiki Central Hospital · Updated on 2013-07-02

19000

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

Sponsors

K

Kurashiki Central Hospital

Lead Sponsor

J

Japanese CTO PCI Expert Registry investigators

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are collecting information on the treatment of chronic total occlusion (CTO) in coronary arteries using percutaneous coronary intervention (PCI). This registry aims to develop a consensus on the best treatment strategies by observing procedures performed by certified Japanese operators. The study is observational and focuses on real-world outcomes of PCI for CTO. The study involves patients who have undergone PCI for CTO lesions in major coronary artery segments or large branches, with occlusions lasting more than three months or of unknown duration. There is no experimental treatment; instead, the registry gathers details about the PCI procedures performed by experts. Patients are followed to assess outcomes after the intervention. Participants will be monitored for successful reopening of blocked arteries without major heart or brain complications shortly after PCI and over a five-year period. The main outcome measured is the absence of major adverse cardiocerebral events during early and long-term follow-ups. The study began in 2013 and will continue through December 2027, with no specific maximum age limit for participants.

CONDITIONS

Brief Title

Japanese CTO PCI Expert Registry

Who Can Participate

Age: 20Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients eligible for PCI
  • Patients who underwent PCI for CTO lesions with TIMI 0
  • CTO occlusion period more than 3 months or unknown
  • CTO in main coronary arteries (segments 1-3, 5-8, 11, 13), large branch vessels (segments 4PL, 9/10, 12), or grafts
Not Eligible

You will not qualify if you...

  • Patients who are ineligible for PCI as judged in clinical practice

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to 1 month after PCI

Participants undergo diagnostic evaluation related to their PCI for CTO procedure.

1 to 2 visits related to PCI procedure

Long-term Monitoring

Duration - Up to 5 years after PCI

Participants are monitored for major adverse cardiocerebral events during long-term follow-up after PCI.

Periodic visits during 5-year follow-up

Trial Site Locations

Total: 1 location

1

Kurashiki Central Hospital

Kurashiki, Japan, 710-8602

Actively Recruiting

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Research Team

K

Keiko Oka

H

Harumi Katoh, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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