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Completed

NCT Number: NCT01873027

OPtical Frequency Domain Imaging vs. INtravascular Ultrasound in Percutaneous Coronary InterventiON

The aim of this randomized study is to evaluate the impact of Optical frequency domain imaging (OFDI) guidance for Percutaneous Coronay Intervention (PCI) with drug-eluting stent (DES) as compared with Intravascular ultrasound (IVUS) guidance.

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Key information

Age range

20 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Wakayama Medical University

Wakayama, 641-8510, Japan

About this study

Optical frequency domain imaging (OFDI) is a novel, high resolution intravascular imaging modality. Intravascular ultrasound (IVUS) is a widely used conventional imaging modality for achieving optimal stent deployment.

The aim of this randomized study is to evaluate the impact of OFDI guidance for Percutaneous Coronay Intervention (PCI) with drug-eluting stent (DES) as compared with IVUS guidance.

We will enroll 800 patients with a de novo lesion who will undergo PCI with DES as is routine practice. Patients will be rondomely assigned to either OFDI-guided PCI arm or IVUS-guided PCI arm.

Patients will then have a follow-up contact at the time of hospital discharge, 8 month and 12 month after PCI.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with a de novo lesion (in the native coronary circulation) and planned to undergo drug-eluting stent implantation for indications according to the Japan and USA guidelines
  • Patients aged between 20 and 85 years old
  • Patients who has provided written informed consent

Exclusion criteria

  • Patients with Acute Myocardial Infarction (AMI) within 3 months
  • Patients with cardiogenic shock
  • Patients with chronic heart failure
  • Patients with renal failure (eGFR <= 30 ml/min/1.73 m2 or Serum creatinine level >=1.5mg/dL)
  • Patients who are currently enrolled in other clinical trial which has possibility to influence the primary endpoint of OPINION trial.
  • Patients planned use of bare metal stent
  • Patients with 3-vessel diseases
  • Planned surgery within 1 year
  • Patient on dialysis
  • Target lesion such as:
  • Left main coronary artery
  • Aorto-Ostial lesion location within 3mm of the aorta junction
  • Chronic total occlusion
  • Small vessel (reference vessel diameter <2.5mm)
  • Coronary artery bypass graft

Treatment and study plan

OFDI

Device
  • OFDI-guided PCI and assessment by OFDI at pre-PCI and post-PCI
  • Follow-up contact at the time of hospital discharge, 8 months and 12months after PCI

Other names: LUNAWAVE, Fastview, Biolimus a9-eluting stent (Nobori stent)

IVUS

Device
  • IVUS-guided PCI and assessment by IVUS at pre-PCI and post-PCI
  • Follow-up contact at the time of hospital discharge, 8 months and 12months after PCI

Other names: VISIWAVE, ViewIT, Biolimus A9-eluting stent (Nobori stent)

Primary outcomes

  1. Target Vessel Failure (TVF)

    Time frame: 12 months after PCI

    The composite endpoint comprised of cardiac death, target vessel-related myocardial infarction (MI) and clinically-driven target vessel revascularization (TVR)

Secondary outcomes

  1. Cardiac death

    Time frame: 12 months after PCI

  2. Myocardial Infarction (MI)

    Time frame: 12 months after PCI

  3. Clinically-driven Target lesion revascularization (TLR)

    Time frame: 12 months after PCI

  4. MACE (composite of cardiac death, MI, TLR)

    Time frame: 12 months after PCI

  5. Target Vessel Revascularization (TVR)

    Time frame: 12 months after PCI

  6. Stroke

    Time frame: 12 months after PCI

  7. Stent thrombosis

    Time frame: 12 months after PCI

  8. Binary restenosis

    Time frame: 12 months after PCI

  9. Renal dysfunction

    Time frame: 8 months after PCI

Sponsors and collaborators

Lead sponsor

Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan

Other

Collaborators

  • Wakayama Medical University

Registry information

Official study title

OPtical Frequency Domain Imaging vs. INtravascular Ultrasound in Percutaneous Coronary InterventiON (OPINION)

Acronym: OPINION

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Jun 7, 2013
Registry last updated
Jul 14, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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