- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02649517
Clinical and Morphological Characteristics of Chronic Inflammation in the Myocardium in Patients With Decompensated HF With Ischemic Systolic Dysfunction (FHID)
Clinical and Morphological Characteristics of Chronic Inflammation in the Myocardium in Patients With Decompensated Heart Failure With Ischemic Systolic Dysfunction
Study Overview
Status
Intervention / Treatment
Detailed Description
Important reason for the development of chronic heart failure is a viral disease of the heart, the three phenotypes associated with: the presence of inflammation without viral agent, implying an autoimmune disease; presence of inflammation and persistent viruses; and the presence of persistent virus without signs of inflammation.
There is a group of patients with coronary heart disease, which on the background of optimal treatment is observed progression of clinical symptoms of coronary heart disease with the subsequent development of heart failure, leading to ischemic cardiomyopathy. Perhaps the reason for this is the combination of inflammatory and ischemic cardiomyopathies.
Inflammatory cardiomyopathy, involved in the pathogenesis of DCM, includes idiopathic, autoimmune and infectious subtypes. Inflammatory disease of the myocardium diagnosed by established histological, immunological and immunohistochemical criteria.
This study will include 60 patients with decompensated heart failure with ischemic left ventricular systolic dysfunction (LVEF <40%) were hospitalized not earlier than 6 months after myocardial revascularization. This group of patients will receive standard treatment, according to national guidelines RSC and ESC, to stabilize heart failure. All patients will be held PCI to exclude ischemic heart failure decompensation. Also, all patients will be performed endomyocardial biopsy as a result of immunohistochemical studies will be made on the separation of the virus and the virus-negative-positive group. After that, the group will be divided into subgroups: virus - and inflammation in the myocardium inflammation without viral antigen, viral inflammation of the presence of antigen and the group with the presence of viral antigen without any signs of inflammation in the myocardium.
The study is nonrandomized.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Vyacheslav Ryabov, MD, Phd
- Phone Number: +73822553689
- Email: rvvt@cardio-tomsk.ru
Study Contact Backup
- Name: Ekaterina Krychinkina, MD
- Phone Number: +73822558360
- Email: katy990@mail.ru
Study Locations
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Tomsk, Russian Federation, 634012
- Recruiting
- Scientific and Research Institution of Cardiology of Siberian Department of RAMS
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Principal Investigator:
- Vyacheslav Ryabov, MD, PhD
-
Contact:
- Vyacheslav Ryabov, MD, Phd
- Phone Number: +73822553689
- Email: rvvt@cardio.tsu.ru
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Tomskii region
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Tomsk, Tomskii region, Russian Federation, 634012
- Recruiting
- Research Institutite for Cardiology
-
Contact:
- Vyacheslav Ryabov, MD, Phd
- Phone Number: +73822553689
- Email: rvvt@cardio-tomsk.ru
-
Principal Investigator:
- Vyacheslav Ryabov, MD, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Men and women over the age of 18 years old and weighing up to 130 kg
- Clinical symptoms of decompensated heart failure in history
- Heart failure decompensation requiring hospitalization for at least 3 of the following symptoms: shortness of breath, or position orthopnea, rales, peripheral edema, jugular venous pulsations, signs of stagnation in the pulmonary circulation according to the X-ray of the chest
- Confirmed coronary heart disease with diastolic dysfunction (LVEF <40%) in history and at the time of admission
- The term of the inclusion of patients in the study did not earlier than six months after revascularization (PCI or CABG)
- Patients receiving medical treatment according to national guidelines RSC and ESC with individually tailored doses of drugs
Exclusion Criteria:
- The refusal of a patient to conduct the necessary studies
- Poor visualization of the heart when ultrasound
- Hemodynamically significant valvular heart disease
- Acute coronary syndrome
- Тhrombosis of the right atrium and right ventricle
- Condition after the operation, impeding access to the right ventricle (cava filters plication vena cava, Mustard or Senning operation on the d-transposition of the great arteries, a mechanical prosthetic tricuspid valve)
- Severe comorbidities
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: chronic inflammation
All patients will be held PCI to exclude ischemic heart failure decompensation.
Also, all patients will be performed endomyocardial biopsy.
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Endomyocardial biopsy will be performed through a puncture in the femoral vein.
3-6 samples taken under the control of myocardial echocardiography or flyuroskopii.
Samples of biopsy material then transmitted Pathomorphology for immunohistochemistry, light microscope.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Incidence of inflammatory infiltrate in the myocardial tissue
Time Frame: 6 month after PCI or CABG
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6 month after PCI or CABG
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Incidence of the virus - positive inflammatory infiltrate in the myocardial tissue
Time Frame: 6 month after PCI or CABG
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6 month after PCI or CABG
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The most frequent viral agents in myocardial tissue in this region
Time Frame: 6 month after PCI or CABG
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6 month after PCI or CABG
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Incidence of the acute myocardial infarction
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Incidence of disturbance rhythm and conduction of the heart
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Left ventricular ejection fraction (Echo)
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Еnd-diastolic volume of the left ventricle (Echo)
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Еnd-systolic volume of the left ventricle (Echo)
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Incidence of the mortality
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Incidence of the stroke
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Incidence of hospitalizations for decompensation heart failure
Time Frame: 6 and 12 month after PCI or CABG
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6 and 12 month after PCI or CABG
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Collaborators and Investigators
Investigators
- Principal Investigator: Vyacheslav Ryabov, MD, PhD, Research Institute for Cardiology
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1801
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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