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Observational Study of OCT in a Patients Undergoing FFR

NCT01663896 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 418

Last updated 2020-07-02

Study results available
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Summary

The purpose of this study is to define and evaluate optical coherence tomography (OCT) stent guidance parameters through prospective data collection in percutaneous coronary intervention (PCI) procedures of de novo lesions.

Conditions

Interventions

DEVICE

OCT stent guidance

Participants undergoing pre- and post-PCI fractional flow reserve (FFR) and OCT

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-11
Primary Completion
2015-03-12
Completion
2015-10-31

Countries

  • United States
  • Australia
  • Austria
  • Belgium
  • Canada
  • China
  • Czechia
  • France
  • Germany
  • Italy
  • Japan
  • Netherlands
  • Spain
  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01663896 on ClinicalTrials.gov