Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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
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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