Stress CMR in Patients With Coronary Chronic Total Occlusions
NCT ID: NCT03152825
Last Updated: 2021-03-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
400 participants
OBSERVATIONAL
2017-05-10
2023-05-31
Brief Summary
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Cardiac MRI (CMR) provide a reliable assessment of both myocardial ischaemia and viability. Using late gadolinium enhancement (LGE) sequences, myocardial segments with LGE \>75% of transmurality do not show any improvement in contractility even after revascularization, representing a subset of patients in which CTO PCI may be futile. Viability assessment by CMR may be also performed with low dose dobutamine infusion; in patients with CTO and akinetic segments, contractility improvement at low dose dobutamine may predict functional recovery in the follow-up. Myocardial ischaemia may be assessed by CMR with high accuracy, identifying perfusion defects during pharmacological-induced hyperemia and/or regional wall motion abnormalities during inotrope infusion.
This study is designed to verify the hypothesis that myocardial ischaemia and viability assessed by CMR could identify patients who are more likely to benefit from PCI in terms of improvement in left ventricular remodeling, functional recovery and clinical outcome.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Viable myocardium Group
At least ONE of the following:
1. Late gadolinium enhancement \<75%.
2. Improvement in segmental function ≥1 grade during low dose dobutamine
PCI
percutaneous coronary intervention attempt
Non-viable myocardium group
At least ONE of the following:
1. Late gadolinium enhancement ≥75%.
2. No improvement in segmental function during low dose dobutamine
PCI
percutaneous coronary intervention attempt
Inducible ischaemia group
At least ONE of the following:
* perfusion defect (≥ 1,5 segments) assessed during peak infusion of adenosine or dobutamine
* new wall motion abnormalities or worsening ≥1 grade during peak infusion of dobutamine
PCI
percutaneous coronary intervention attempt
Non-inducible ischaemia group
None of conditions qualifying for the "Inducible ischemia group"
PCI
percutaneous coronary intervention attempt
Interventions
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PCI
percutaneous coronary intervention attempt
Eligibility Criteria
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Inclusion Criteria
* baseline stress CMR
* signed informed consent
Exclusion Criteria
* severe CKD
* contraindications to adenosine or dobutamine
* unable/unwilling to sign informed consent
* pregnancy
18 Years
ALL
No
Sponsors
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Ospedale San Donato
OTHER
Responsible Party
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Massimo Lombardi
Director of Multimodality Cardiac Imaging Unit
Principal Investigators
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Massimo Lombardi, MD
Role: PRINCIPAL_INVESTIGATOR
Policlinico San Donato
Locations
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IRCCS Policlinico San Donato
San Donato Milanese, Milan, Italy
Countries
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Central Contacts
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Facility Contacts
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Silvia Pica, MD
Role: primary
References
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Other Identifiers
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CARISMA_CTO
Identifier Type: -
Identifier Source: org_study_id
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