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Evaluation of new image processing software that supports percutaneous coronary intervention

Evaluation of new image processing software that supports percutaneous coronary intervention - Evaluation of new image processing software that supports percutaneous coronary intervention

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000017554
Enrollment
30
Registered
2015-05-14
Start date
2012-06-13
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

The University of Tokyo Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) patients who undertake percutaneous coronary intervention 2) patients with elective cases 3) patients who are over 20 years old when informed consent are collected 4) patients from whom informed consent are collected with adequate understanding of the research

Exclusion criteria

Exclusion criteria: 1) patients with 3 vessel disease 2) patients with left main trunk disease 3) patients with total occlusion disease 4) patients who should not undertake IVUS 5) women who are or are likely to be pregnant or nursing 6) patients whom primary investigators or sub investigators decide to exclude because of inadequacies for the study

Design outcomes

Primary

MeasureTime frame
Accuracy of Co-retgistration between angiographic images and IVUS images

Secondary

MeasureTime frame
radiation dose 1) radiation dose of fluoroscopy during pullback of IVUS 2) total radiation dose in each case

Countries

Japan

Contacts

Public ContactJiro Ando

The University of Tokyo Hospital Department of Cardiovascular Medicine

jando-kkr@umin.ac.jp+81-3-3815-5411

Outcome results

None listed

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