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The FAST OCT Study

NCT04683133 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2020-12-24

No results posted yet for this study

Summary

This trial is designed to associate angiography-based fractional flow reserve (3D-angio-based FFR) values with optical coherence tomography findings in pre- and post-percutaneous coronary intervention in patients with non-ST segment elevation acute coronary syndromes.

Conditions

  • Tomography, Optical Coherence
  • Myocardial Revascularization
  • NSTEMI - Non-ST Segment Elevation MI
  • Unstable Angina
  • Coronary Arteriosclerosis
  • 3D-angio-based FFR

Interventions

DIAGNOSTIC_TEST

Optical coherence tomography assessment

Optical coherence tomography assessment of coronary arteries with intermediate to severe stenosis

Sponsors & Collaborators

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-12-01
Primary Completion
2021-12-31
Completion
2021-12-31
FDA Device
Yes

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Companies

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 NCT04683133 on ClinicalTrials.gov