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Integrazione di lisato probiotico (postbiotico e metabiotico) per pazienti adulti con MASLD (studio DELI_MASLD)

21 settembre 2026 aggiornato da: Nazarii Kobyliak, Bogomolets National Medical University

Efficacia e sicurezza della supplementazione di lisato probiotico (postbiotico e metabiotico) nei pazienti adulti con MASLD

The current study aim was to conduct placebo-controlled randomize clinical trial to assess the short-term efficacy and safety of postbiotics on hepatic fat content as measured by biochemichal hepatic steatosis indeces, serum lipid profile, transaminases activity and chronic systemic inflammatory markers in MASLD patients.

The study will include 3 periods. Screening period of up to 1 weeks to assess the eligibility to inclusion/exclusion criteria. Treatment period for 3 month where the participants will receive a twice daily oral dose of postbiotics (cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023) at the assigned dose of 100mg or placebo in capsules. During this period monthly phone contacts will be done for assessment of compliance and safety concerns. Follow-up period of up to 3 month.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

The scientific literature points to the beneficial properties of probiotics in the process of regulating metabolism, yet at the same time, some scientific papers question the effectiveness and the safety of probiotics. In turn, postbiotics and metabiotics are preparations of inanimate microorganisms and / or their components, which are directly identified with the safety of their use and the health benefits of the host. Due to the chemical structure of postbiotics and metabiotics, it is found that they have many health benefits; in particular, they have a local effect on certain tissues of the intestinal epithelium, and influence on many other organs and tissues. It is postbiotics metabolites and metabiotics structural cell fragments that create the appearance of a therapeutic effect of probiotics, which, in turn, limits the risk of introducing living microorganisms into a weakened immune defence. It should also be pointed out that postbiotics and metabiotics are more stable and have a longer shelf-life.

The practical use of probiotics and the study of the mechanism of their action made lately to find that a certain level of biological activity is preserved by dead probiotic cells and even their lysates, which are the natural mixes of metabiotic and postbiotic substances; a biological activity which is strongly oriented toward gut health and immune system regulation. Because probiotic lysates demonstrated biological activity without any of the potential adverse side effects associated with live bacterial cells, one of the future goal is research of the novel postbiotics and metabiotics substances, their individual structures and biological characteristics for understanding their way of communications with host cells and microbiota representatives.

Considering the high biological activity and safety of postbiotics and metabiotic substances, it can be concluded that such a treatment vector will be promising in the near future. That's why our investigation will concentrate on postbiotic, a supplement containing dry fermented cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023.

Recent scientific animal studies on the stated issues point to the benefits of some postbiotics in treating metabolic disorders. The current study aim was to conduct placebo-controlled randomize clinical trial to assess the short-term efficacy and safety of postbiotics on hepatic fat content as measured by biochemichal hepatic steatosis indeces, serum lipid profile, transaminases activity and chronic systemic inflammatory markers in MASLD patients.

The study will include 3 periods. Screening period of up to 1 weeks to assess the eligibility to inclusion/exclusion criteria. Treatment period for 3 month where the participants will receive a twice daily oral dose of postbiotics (cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023) at the assigned dose of 100mg or placebo in capsules. All capsules will be identical with similar organoleptic characteristics (e.g., taste and appearance). Follow-up period of up to 3 month.

The pre-randomization period will be designed to minimize the effects of dietary changes on metabolic markers. For this purpose, 2 weeks before the study start, after inform consent signed, patients were instructed in one-on-one sessions with a dietitian to follow a therapeutic lifestyle-change diet as classified by the NCEP. In addition, participants were instructed to continue with stable anti-hyperglycemic treatment and received standardized mild physical training for 1 hour per day.

Patients who underwent the study were instructed to take the trial medication as prescribed. Throughout the study, weekly phone follow-up visits were provided for assessment of compliance, adherence to the protocol, as well as the recording of adverse events. The effectiveness of therapy was compared and evaluated separately in the two groups.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

52

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Kyiv, Ucraina, 01601
        • Bogomolets National Medical University
      • Kyiv, Ucraina, 01601
        • Taras Shevchenko National University of Kyiv
      • Kyiv, Ucraina, 01601
        • Kyiv City Clinical Endocrinology Center
      • Kyiv, Ucraina, 02000
        • Center for Innovative Medical Technologies of the National Academy of Sciences of Ukraine
      • Lviv, Ucraina, 79010
        • Danylo Halytsky Lviv National Medical University

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 70 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • adult participants (ages 18-70)
  • presence of MASLD according to "A multisociety Delphi consensus statement", 2023;
  • the diagnosis of fatty liver was based on the results of abdominal ultrasonography. Of 4 known criteria (hepato-renal echo contrast, liver brightness, deep attenuation, and vascular blurring), the participants were required to have hepato-renal contrast and liver brightness to be given a diagnosis of SLD
  • fatty liver index (FLI) more than 60;
  • BMI 25-39.9 kg/m2;
  • aspartate transaminase (AST) and alanine transaminase (ALT) ≤3x upper limit of normal;
  • written informed consent.

Exclusion Criteria:

  • recent hepatitis, or positive screening test for hepatitis B (hepatitis B virus surface antigen) or hepatitis C (hepatitis C antibody);
  • alcohol abuse (>20 g/day (2 standard drinks) in women or > 30 g/d (3 drinks) in men over a two-year period);
  • drug-induced liver disease, Wilson's disease, hereditary deficiency of antitrypsin-1 and idiopathic hemochromatosis;
  • history of decompensated liver disease including ascites, encephalopathy or variceal bleeding;
  • regular use of an agents with gut microbiota modulation activity (antibiotic, pro-, pre-, post or synbiotics supplement etc.) within 3 months prior to enrollment;
  • allergy on probiotics or their components;
  • use of agents such as vitamin E, omega-3 fatty acids or medications with evidence for effects on NAFLD (pioglitazone, GLP-1 analogues, dipeptidyl peptidase IV inhibitors, ursodeoxycholic acid);
  • subjects with a history of bariatric surgery or significant weight loss (> 5% body weight) or rapid weight loss (> 1.6kg/week), within 6 months prior to enrollment;
  • uncontrolled cardiovascular or respiratory disease, decompensated liver disease including ascites, encephalopathy or variceal bleeding, active malignancy, or chronic infections;
  • participant who had severe course of COVID-19 (extracorporeal membrane oxygenation, mechanically ventilated), and/or had a confirmed case of COVID-19 within 4 weeks prior to enrollment;
  • participation in other clinical trials;
  • presence of pregnancy or lactation.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Probiotic lysate (postbiotic and metabiotc) group

oral, 2 capsules per day (BID) for 3 month treatment

Each capsule contains 100 mg of cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023 in powder

Comparatore placebo: Placebo group

placebo, oral, 2 capsules per day (BID) for 3 month treatment

Placebo

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
changes in fatty liver index (FLI)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

FLI = [e 0.953*loge (triglycerides) + 0.139*BMI + 0.718*loge (ggt) + 0.053*waist circumference - 15.745) / (1 + e 0.953*loge (triglycerides) + 0.139*BMI + 0.718*loge (ggt) + 0.053*waist circumference - 15.745)] × 100

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
hepatic steatosis index (HSI)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

HSI = 8 x ALT/AST + BMI(+ 2 if type 2 diabetes yes, + 2 if female)

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
TyG index
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

TyG = ln [Fasting triglyceride (mg / dl) x Fasting glucose (mg / dl)] / 2

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Concentration of AST
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

AST in IU/L

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
Concentration of ALT
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

ALT in IU/L

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
Concentration of Gamma-glutamyl Transferase (GGT)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

GGT in IU/L

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
Concentration of Total Cholesterol (TC)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

TC in mmol/l

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
Concentration of Tryglicerides (TG)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

TG in mmol/l

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
Concentration of high sensitivity CRP (hs-CRP)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

hs-CRP in mg/L

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
waist circumferences (WC)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

WC in cm

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
body mass index (BMI)
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

weight in kg and height in meters will be combined to report BMI in kg/m^2

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
visceral fat content
Lasso di tempo: at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

visceral fat content using electronic scales-analyzers of body composition Tanita Scale BC-601

at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 maggio 2024

Completamento primario (Effettivo)

31 dicembre 2024

Completamento dello studio (Effettivo)

31 gennaio 2025

Date di iscrizione allo studio

Primo inviato

2 aprile 2024

Primo inviato che soddisfa i criteri di controllo qualità

2 aprile 2024

Primo Inserito (Effettivo)

8 aprile 2024

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

23 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

21 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • DELI_MASLD

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

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 .