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Etiologic Mechanisms, Myocardial Changes and Prognosis of Patients With MINOCA

Primary Purpose

Myocardial Infarction With Nonobstructive Coronary Arteries

Status
Unknown status
Phase
Not Applicable
Locations
Lithuania
Study Type
Interventional
Intervention
extended clinical, laboratory and instrumental examination; treatment options comparison
Sponsored by
Vilnius University Hospital Santaros Klinikos
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Myocardial Infarction With Nonobstructive Coronary Arteries

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. acute MI:

    • detection of a rise and/or fall of cardiac troponin(cTn) values with at least one value above the 99th percentile upper reference limit (URL) and with at least one of the following:
    • symptoms of acute myocardial ischaemia;
    • new ischaemic ECG changes;
    • development of pathological Q waves;
    • imaging evidence of new loss of viable myocardium or new regional wall motion abnormality in a pattern consistent with an ischaemic aetiology
  2. non-obstructive coronary arteries on angiography:

    - the absence of obstructive coronary artery disease (CAD) on angiography, (i.e. no coronary artery stenosis ≥50%), in any potential infarct-related artery;

    This includes both patients with:

    • normal or near normal coronary arteries (no stenosis >30%)
    • mild coronary atheromatosis (stenosis >30% but <50%).
  3. angiography performed within 24 - 48 hours
  4. age >18 years
  5. informed consent

Exclusion Criteria:

  • acute kidney failure
  • stage 4-5 chronic kidney disease
  • contraindications for coronary angiography or CMR
  • patients involved in another biomedical trial
  • inability to make a decision to participate in the investigation

Sites / Locations

  • Vilnius University Hospital Santaros klinikosRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

MINOCA (group I) - conventional MI treatment

MINOCA (group II)

Arm Description

Traditional MI treatment with optimal doses of statin, angiotensin-converting enzyme inhibitors (ACEI) or angiotensin II receptor blockers (ARB), beta-blockers (BB) and dual antiplatelet therapy (DAPT).

Treatment with a low-dose statin and ACEI/ARB. In case of vasospasm, calcium channel blockers.

Outcomes

Primary Outcome Measures

Rate of all-cause mortality
Rate of cardiovascular death

Secondary Outcome Measures

Rate of hospitalization for MI
Rate of MACE

Full Information

First Posted
August 27, 2020
Last Updated
September 3, 2020
Sponsor
Vilnius University Hospital Santaros Klinikos
Collaborators
Research Council of Lithuania
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1. Study Identification

Unique Protocol Identification Number
NCT04538924
Brief Title
Etiologic Mechanisms, Myocardial Changes and Prognosis of Patients With MINOCA
Official Title
Multimodality Study on Etiologic Mechanisms, Myocardial Changes, and Prognosis of Patients With Myocardial Infarction With Non-obstructive Coronary Arteries
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
January 1, 2023 (Anticipated)
Study Completion Date
January 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vilnius University Hospital Santaros Klinikos
Collaborators
Research Council of Lithuania

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This prospective trial will include 150 patients with myocardial infarction with non-obstructive coronary arteries (MINOCA). A thorough clinical, laboratory and imaging evaluation will be performed by novel biomarkers and modern imaging techniques (heart magnetic resonance imaging and noninvasive testing). Moreover, two different treatment groups will be distinguished. Additionally, a retrospective analysis of patients meeting MINOCA criteria will be performed.
Detailed Description
Primary goals The primary trial goal is to assess the etiologic mechanisms of myocardial damage in patients with MINOCA as well as to evaluate a variety of therapeutic strategies for these patients. Secondary goals To assess functional and morphological myocardial changes in patients with MINOCA; To assess the true prevalence and prognostic relevance of MINOCA (all-cause mortality and MACE); To test the effect of conventional acute MI therapies (BB, ACEI, ARB, CCB, statins, anti-platelet agents) on MACE (death and myocardial infarction) and all-cause mortality in patients with MINOCA; To test the diagnostic and prognostic role of several biomarkers (sST2, BNP, cTnI, CRP, copeptin, procalcitonin, MR-proADM, galectin-3) in patients with MINOCA; To assess the impact of MINOCA with respect to chronic health status, such as persistent angina symptoms, impairment in quality of life, and depression; To evaluate systemic microcirculation status and assess its effect on long term outcomes. To evaluate hospital mortality and all-cause death within 6 and 12 months follow-up; To determine recurrent hospitalizations within 30-days, 6 and 12 months follow-up; To assess peak creatine kinase, creatine kinase-MB and troponin levels during hospital stay; To determine quality of life at 6 and 12 months assessed using the Euroqol 5D (EQ-5D) questionnaire (www.euroqol.org).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction With Nonobstructive Coronary Arteries

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MINOCA (group I) - conventional MI treatment
Arm Type
Other
Arm Description
Traditional MI treatment with optimal doses of statin, angiotensin-converting enzyme inhibitors (ACEI) or angiotensin II receptor blockers (ARB), beta-blockers (BB) and dual antiplatelet therapy (DAPT).
Arm Title
MINOCA (group II)
Arm Type
Other
Arm Description
Treatment with a low-dose statin and ACEI/ARB. In case of vasospasm, calcium channel blockers.
Intervention Type
Other
Intervention Name(s)
extended clinical, laboratory and instrumental examination; treatment options comparison
Intervention Description
Multimodality investigation and different treatment comparison
Primary Outcome Measure Information:
Title
Rate of all-cause mortality
Time Frame
12 months follow-up
Title
Rate of cardiovascular death
Time Frame
12 months follow-up
Secondary Outcome Measure Information:
Title
Rate of hospitalization for MI
Time Frame
12 months follow-up
Title
Rate of MACE
Time Frame
12 months follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: acute MI: detection of a rise and/or fall of cardiac troponin(cTn) values with at least one value above the 99th percentile upper reference limit (URL) and with at least one of the following: symptoms of acute myocardial ischaemia; new ischaemic ECG changes; development of pathological Q waves; imaging evidence of new loss of viable myocardium or new regional wall motion abnormality in a pattern consistent with an ischaemic aetiology non-obstructive coronary arteries on angiography: - the absence of obstructive coronary artery disease (CAD) on angiography, (i.e. no coronary artery stenosis ≥50%), in any potential infarct-related artery; This includes both patients with: normal or near normal coronary arteries (no stenosis >30%) mild coronary atheromatosis (stenosis >30% but <50%). angiography performed within 24 - 48 hours age >18 years informed consent Exclusion Criteria: acute kidney failure stage 4-5 chronic kidney disease contraindications for coronary angiography or CMR patients involved in another biomedical trial inability to make a decision to participate in the investigation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rokas Šerpytis
Phone
+37061089860
Email
rserpytis@gmail.com
Facility Information:
Facility Name
Vilnius University Hospital Santaros klinikos
City
Vilnius
ZIP/Postal Code
LT-08406
Country
Lithuania
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rokas Šerpytis
Phone
+37061089860
Email
rserpytis@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34562410
Citation
Serpytis R, Majauskiene E, Navickas P, Lizaitis M, Glaveckaite S, Rucinskas K, Petrulioniene Z, Valeviciene N, Samalavicius RS, Berukstis A, Baranauskas A, Gargalskaite U, Laucevicius A, Chen QM, Alpert JS, Serpytis P. Randomized Pilot Trial on Optimal Treatment Strategy, Myocardial Changes, and Prognosis of Patients with Myocardial Infarction with Nonobstructive Coronary Arteries (MINOCA). Am J Med. 2022 Jan;135(1):103-109. doi: 10.1016/j.amjmed.2021.08.023. Epub 2021 Sep 22.
Results Reference
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Etiologic Mechanisms, Myocardial Changes and Prognosis of Patients With MINOCA

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