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Motion and IntraCoronary Ecg Ischemia Development Study (MICE)

Motion and IntraCoronary Ecg Ischemia Development Study (MICE)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04061525
Acronym
MICE
Enrollment
30
Registered
2019-08-19
Start date
2019-02-01
Completion date
2024-01-31
Last updated
2019-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischaemic Heart Disease

Brief summary

The concept of the ischemic cascade is generally accepted hypothesis, according to which whenever ischemia of the myocardium occurs there is a consequence of events, that always occur in a given order - diastolic dysfunction first, followed by systolic dysfunction, then changes on electrocardiogram (ECG) and finally chest pain sensation. The occurrence of every next stage of cascade means more severe ischemia and respectively - more severe myocardial damage. We propose that mechanical and electrical changes in the myocardium during ischemia appear simultaneously.

Detailed description

The development of an ischemic event, whether silent or painful, represents the cumulative impact of a sequence of pathophysiologic events. Each ischemic episode is initiated by an imbalance between myocardial oxygen supply and demand that may ultimately be manifested as angina pectoris. The ischaemic cascade is the concept that progressive myocardial oxygen supply-demand mismatch causes a consistent sequence of events, starting with metabolic alterations and followed sequentially by myocardial perfusion abnormalities, wall motion abnormalities, ECG changes, and angina. This concept would suggest that investigations that detect expressions of ischaemia earlier in the cascade should be more sensitive tests of ischaemia than those that detect expressions appearing later in the cascade.Visualization of a regional decrease in the systolic movement of the endocardium and a decrease in myocardial thickening are the main principles for the diagnosis of myocardial damage. However, the concept of ischaemic cascade is entirely based on clinical observations. It is not clear, which changes (mechanical or electrical) appear first during an episode of ischemia and which are prognostically more important. The objective of this study is to compare ischemic cascade towards ischemic constellation regarding beginning, duration and sequence of the electric, kinetic and haemodynamic signs of ischemia by FFR, icECG and wall motion abnormalities sign (M-sign - deformation and shortening of the wire tip) in patients with coronary bifurcation stenosis

Interventions

PROCEDUREPercutaneous coronary intervention with FFR measurement and intracoronary ECG registration

Measurement of fractional flow reserve (FFR), registration of intracoronary ECG and radioscopic registration of wire tip movement in the main and in the side branch in the beginning, at the end and during every step of coronary bifurcation percutaneous intervention.

Sponsors

University National Heart Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Subject at least 18 years of age. * Subject able to verbally confirm understandings of risks, benefits of receiving PCI for true bifurcation lesions, and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure. * Target main branch lesion(s) located in a native coronary artery with diameter of ≥ 2.5 mm and ≤ 4.5 mm. Target side branch lesion(s) located in a native coronary artery with diameter of ≥ 2.0 mm. * Target lesion(s) amenable for PCI with balloon angioplasty of the side branch.

Exclusion criteria

* Subjects with significant ST-T change (≥ 1mm). * Non-cardiac co-morbid conditions are present with life expectancy \<1 year or that may result in protocol non-compliance (per site investigator's medical judgment). * Subjects who refuse to give informed consent. * Subjects with the following angiographic characteristics: left main coronary artery stenosis, total occlusion before occurrence of SB, lesion of interest located at infarct-related artery. * Subjects with LVEF \< 30%. * Subjects with moderate or severe degree valvular heart disease or primary cardiomyopathy. * LBBB, RBBB, atrial fibrillation/flutter with no identifiable isoelectric line.

Design outcomes

Primary

MeasureTime frameDescription
Side branch region ischemiaPercutaneous coronary intervention procedure time (up to 4 hours)Beginning, duration, sequence of the electric, kinetic and haemodynamic signs of ischemia, comparison between ischemic cascade and constellation.

Secondary

MeasureTime frameDescription
Target lesion revascularization12 monthsAny revascularization at the territory of previously intervention
Number of patients not alive12 monthsNumber of patients not alive
Myocardial infarction after hospital discharge12 monthsMyocardial infarction according to universal definition of MI - CK-MB \> 2xULN +/- symptoms +/- surface ECG changes in at least 2 leads
New onset angina or heart failure symptoms12 monthsNew onset angina symptoms of at least CCS class II; New onset dyspnea at exertion or at rest

Other

MeasureTime frameDescription
Periprocedural myonecrosis - extent of post PCI enzyme elevation48 hoursTroponin I elevation 1-3; 3-5; \>5 x ULN Creatin phosphokinase MB fraction elevation 1-3; 3-5; \>5 x ULN

Countries

Bulgaria

Contacts

Primary ContactDobrin Vassilev
dobrinv@gmail.com+359886846550

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026