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Clinical Trials/NCT04444037
NCT04444037
Completed
Not Applicable

Impact of Optical Coherence Tomography Imaging on Decision-making During Percutaneous Coronary Intervention in Patients Presented With Acute Coronary Syndromes

Assiut University1 site in 1 country390 target enrollmentJanuary 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Coronary Syndrome
Sponsor
Assiut University
Enrollment
390
Locations
1
Primary Endpoint
Percent difference in lumen expansion in stent treated lesion
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Optical coherence tomography (OCT) provides valuable information to guide percutaneous coronary intervention (PCI) in acute coronary syndrome (ACS) regarding lesion preparation, stent sizing, and stent optimization.

Detailed Description

OCT can be used in acute coronary syndrome (ACS). ACS has more complex culprit lesion morphologies and larger extent of coronary atherosclerosis compared with stable coronary artery disease. The detailed vascular information obtained by OCT may impact PCI in ACS, and which may improve acute results and late outcomes of PCI. Stent expansion immediately after PCI is a strong predictor of late outcomes of PCI, and it is associated with late clinical outcomes in many previous trials.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
April 30, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amir Khalifa Mahfouz Khalifa

Principle investigator, Cardiology department

Assiut University

Eligibility Criteria

Inclusion Criteria

  • Patients presented with acute coronary syndrome.
  • PCI was done to them with stent implantation.

Exclusion Criteria

  • Multivessel PCI at the index procedure.
  • Patients with ACS due to graft failure post CABG.
  • Patients treated with no stent implantation.

Outcomes

Primary Outcomes

Percent difference in lumen expansion in stent treated lesion

Time Frame: Immediately after the procedure

Compare residual percent diameter stenosis, percent area stenosis, and acute lumen gain between the two groups.

Secondary Outcomes

  • Clinical outcomes at 1 year follow up(During 1 year following the index procedure)

Study Sites (1)

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