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Single-centre, Registry Trial, the Patients Presented With Stable Coronary Artery Disease

NCT02364778 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2016-07-07

Study results available
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Summary

This is a prospective study to analyze the outcome of provisional main vessel stenting on side branch by utilizing Two-Dimensional (2D) and Three-Dimensional (3D) frequency domain optical coherence tomography (FD-OCT). To analyze the fate of side-branch after provisional main vessel stenting based on morphology defined prior to PCI by OCT. Offline analysis of side branch impingement of the ostium of SB leading to acute loss in SB diameter area, carina shift and plaque shift will be also be performed.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Annapoorna Kini, MD · Icahn School of Medicine at Mount Sinai

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2015-05-31
Completion
2015-05-31

Countries

  • United States

Study Locations

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Entities

Diseases
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 NCT02364778 on ClinicalTrials.gov