- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT04820556
Gut Microbiota in Chronic Noncommunicable Diseases
The Development of Preventive Methods for Chronic Noncommunicable Diseases Based on Modulation of Gut Microbiota Composition and Function
Panoramica dello studio
Stato
Tipo di studio
Iscrizione (Effettivo)
Contatti e Sedi
Luoghi di studio
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Moscow, Federazione Russa, 101990
- National Medical Research Center for Therapy and Preventive Medicine of the Ministry of Healthcare of the Russian Federation
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Moscow, Federazione Russa, 119121
- Centre for Strategic Planning and Management of Biomedical Health Risks of the Federal Medical Biological Agency
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Metodo di campionamento
Popolazione di studio
Descrizione
Criteria for groups with arterial hypertension, chronic obstructive pulmonary disease (COPD), asthma, type 2 diabetes mellitus and nonalcoholic fatty liver disease (NAFLD) (both prospective and retrospective)
Inclusion criteria:
All mentioned groups:
- Men and women aged ≥ 18 and <80
- Signed informed consent form
Group of arterial hypertention (inclusion criteria):
- No current treatment of hypertension
- Systolic blood pressure <180 mm Hg and diastolic blood pressure <110 mm Hg
- No clinical signs of other cardiovascular diseases
Group of COPD and asthma (inclusion criteria)
- Medical records, confirming COPD or asthma
- Regular stable treatment of COPD, asthma or any chronic disease for ≥ 4 weeks before the enrollment. If inhaled corticosteroids are being used, regular treatment is required for ≥12 weeks.
- Absence of acute exacerbations of COPD, asthma or any concomitant diseases 4 weeks before the enrollment
- No use of genetically engineered biological drugs
- For patients with COPD after inhalation of salbutamol (400 mcg) the ratio FEV1/FVC is less than 0,70
Group of type 2 diabetes mellitus (inclusion criteria)
- Confirmed type 2 diabetes mellitus
- Stable glucose lowering treatment for ≥ 1 month
- No systemic corticosteroid treatment 4 weeks before the enrollment
Group of NAFLD (inclusion criteria)
- Ultrasound criteria of non-alcoholic fatty liver disease or
- Confirmed non-alcoholic fatty liver disease using FibroMax test
Control group inclusion criteria
- Men and women aged ≥ 18 and <80 years
- Signed informed consent form
Control group for arterial hypertension (inclusion criteria):
1. No history of cardiovascular diseases, COPD or asthma
Control group for COPD and asthma (inclusion criteria):
1. No history of diabetes mellitus, NAFLD, COPD and asthma
Exclusion criteria for all groups
- Age < 18 years and ≥80 years
- Denial of further participation
- Obesity with BMI≥40 kg/m2
- History of organ transplantion
- Psychiatric disorder, limiting participation in the study
- Acute infections
- Exacerbation of chronic infection 2 weeks before the enrollment
- Cancer with no radical treatment
- Pregnancy and lactation
- Alcohol and drug addition
- Chronic kidney disease with GFR <30 ml/min/1.73m2
- Systemic autoimmune diseases
- Inflammatory bowel disease
- Antimicrobial and probiotic treatment 3 months before the enrollment
Additional exclusion criteria adjusted for each group
Group of arterial hypertension (exclusion criteria):
- Ischemic heart disease (angina pectoris, myocardial infarction), cerebrovascular disease (stroke, transient ischemic attack), occlusive peripheral arterial disease, revascularization of any vascular bed.
- Cardiomyopathies
- Symptomatic arterial hypertension
- Diabetes mellitus
- Signs of previous myocardial infarction on ECG
- Arrhythmias (parohysmal arrhythmias, atrial fibrillation, sinoatrial block, atrioventricular block grade II-III)
- Signs of current myocardial ischemia on ECG
- Decompensated heart failure
Group of COPD and asthma (exclusion criteria):
Exacerbation of COPD or asthma 3 months before the enrollment which required antibiotic treatment or systemic corticosteroids.
Group of type 2 diabetes mellitus (exclusion criteria):
- Type 1 diabetes mellitus and other specific types of diabetes
- Severe microangiopathy: proliferative and terminal stage of diabetic retinopathy, chronic kidney disease (GFR < 30 ml/min/1,73 m2) for patients with type 2 diabetes
- The history of moderate, severe and very severe COPD
- The history of moderate or severe asthma
- Vegetarians or vegans
Group of non-alcoholic fatty liver disease (exclusion criteria):
- Chronic liver diseases except NAFLD
- The history of moderate, severe and very severe COPD
- The history of moderate or severe asthma
- Vegetarians or vegans
- Diabetes mellitus
Criteria for groups of heart failure and obstructive atherosclerosis (retrospective)
Inclusion criteria for HF-pEF group:
- Men and women aged ≥ 18 and <80 years
- Signs and symptoms of heart failure
- Left ventricular diastolic dysfunction
- Left ventricular ejection fraction ≥50%
- NT-pro BNP >125 pg/ml
- Signed study informed consent form
Inclusion criteria for HF-rEF group:
- Men and women aged ≥ 35 and <80 years
- Signs and symptoms of heart failure
- Left ventricular ejection fraction <50%
- Signed study informed consent form
Inclusion criteria for obstructive atherosclerosis group:
- Men and women aged ≥ 35 and <80 years
Symptoms and signs of obstructive atherosclerosis of any vascular bed:
- Ischemic heart disease or
- Revascularization of coronary, renal, brachiocephalic or lower extremity arteries or
- carotid endarterectomy or
- chronic lower extremity ischemia or
- history of myocardial infarction, stroke, transient ischemic attack or
- renovascular AH
- atherosclerotic aorta aneurysm
- Signed study informed consent form
Inclusion criteria for control group for HF-pEF, HF-rEF and obstructive atherosclerosis
- Men and women aged ≥ 18 and <80 years.
- No signs or symptoms of chronic heart failure
- No signs of left ventricular diastolic dysfunction
- No history, signs or symptoms of obstructive atherosclerosis of any vascular bed
- Signed study informed consent form
Exclusion criteria for groups with HF-pEF, HF-rEF and obstructive atherosclerosis:
- Age <18 and ≥80 years.
- Refuse to sign study informed consent form
- Body mass index ≥35 kg/m2
- Chronic kidney disease with GFR <30 ml/min/1,73 m2
- Current smoking
- Moderate or severe COPD
- Moderate or severe asthma
- Acute infections or exacerbation of chronic infections 2 weeks prior to study enrollment
- History of allergic reactions to gadolinium contrast
- Hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy: primary, amyloidosis, glycogen storage diseases, hemochromatosis, sarcoidosis, drug induced cardiomyopathy, radiation heart disease, constrictive pericarditis).
- Connective tissue disease
- Cancer with no radical treatment
- Pregnancy or lactation
- Inflammatory bowel disease
- Use of antimicrobial agents, probiotics or systemic corticosteroids 3 months before the enrollment
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
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Gruppo di controllo
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Arterial hypertension
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Atherosclerosis occlusive disease
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Heart failure with preserved ejection fraction
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Heart failure with reduced ejection fraction
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Diabetes mellitus, type 2
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Chronic obstructive pulmonary disease and asthma
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Nonalcoholic fatty liver disease
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
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Significant (p<0,05) correlation (r>0,5) between abundance of Faecalibacterium genus and concentration of lipopolysaccharide
Lasso di tempo: on enrollment
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on enrollment
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Collaboratori e investigatori
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie dell'apparato digerente
- Processi patologici
- Malattie cardiache
- Malattia cardiovascolare
- Malattie vascolari
- Disturbi del metabolismo del glucosio
- Malattie metaboliche
- Malattie delle vie respiratorie
- Arteriosclerosi
- Malattie arteriose occlusive
- Malattie polmonari
- Malattie del sistema endocrino
- Attributi della malattia
- Diabete mellito
- Malattie del fegato
- Arresto cardiaco
- Ipertensione
- Diabete mellito, tipo 2
- Malattie polmonari, ostruttive
- Fegato grasso
- Malattia del fegato grasso non alcolica
- Aterosclerosi
- Malattie non trasmissibili
Altri numeri di identificazione dello studio
- 3162021
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .