Clinical comparison study between newly developed FFR device based on optical interferometry and conventional FFR device

Clinical comparison study between newly developed FFR device based on optical interferometry and conventional FFR device - Clinical evaluation study with FFR device based on optical interferometer

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000028268

Enrollment

Registered

2017-08-01

Start date

2017-08-01

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 patients

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. intermediate coronary stenosis 2. more than 20 years old

Exclusion criteria

Exclusion criteria: 1. AV block 2. bronchial asthma

Design outcomes

Primary

Measure	Time frame
1. Evaluation of Safety use of newly FFR devise 2. Evaluation of Fractional Flow Reserve	—

Countries

Japan

Contacts

Public ContactSuzuki Akihiro

Aichi Medical University cardiology

akis820@aichi-med-u.ac.jp0561623311

Outcome results