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Clinical Trials/NCT05170971
NCT05170971
Recruiting
Not Applicable

The Clinical Efficacy and Safety of Fecal Microbiota Transplantation in Patients With Acute-on-chronic Liver Failure

Ningbo Medical Center Lihuili Hospital1 site in 1 country60 target enrollmentMay 1, 2021
ConditionsLiver Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Liver Failure
Sponsor
Ningbo Medical Center Lihuili Hospital
Enrollment
60
Locations
1
Primary Endpoint
Coagulation function change
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

To investigate the safety, adverse reactions and therapeutic effects of fecal microbiota transplantation on patients with liver failure;to investigate the effect of fecal microbiota transplantation on the intestinal microecology and "gut-liver axis immune system" of liver failure, and further optimization of fecal microbiota transplantation technology.

Registry
clinicaltrials.gov
Start Date
May 1, 2021
End Date
December 31, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Ningbo Medical Center Lihuili Hospital
Responsible Party
Principal Investigator
Principal Investigator

xulanman

Head of Infection Department

Ningbo Medical Center Lihuili Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients willing to sign informed consent
  • Patients aged 18-65
  • According to the diagnosis standard of liver failure in the guide for diagnosis and treatment of liver failure (2018 Edition), the eligible patients are included, that is, on the basis of chronic liver disease, the syndrome with acute jaundice deepening and coagulation dysfunction as the manifestation of liver failure caused by various inducements can be combined with complications such as Hepatoencephalopathy, ascites, electrolyte disorder, infection, hepatorenal syndrome, hepatopulmonary syndrome, etc And extrahepatic organ failure. The patient's jaundice deepened rapidly, the serum TBIL ≥ 10 × ULN or the daily rise ≥ 17.1 μ mol / L; there was bleeding, PTA ≤ 40% (or INR ≥ 1.5)

Exclusion Criteria

  • Patients with severe heart failure, COPD, cerebrovascular accident, nephrotic syndrome, etc;
  • Patients with gastrointestinal bleeding, pulmonary infection, septicemia, etc
  • Patients with liver cancer, lung cancer, lymphoma and other malignant tumors
  • Patients taking anticoagulants, mental diseases and immune diseases for a long time
  • Pregnant or lactating women.

Outcomes

Primary Outcomes

Coagulation function change

Time Frame: Blood samples were collected 1 week before faecal bacteria transplantation, and followed up at 5 day, 10 day, 15 day, 20 day, 4 and 8 weeks after faecal bacteria transplantation, respectively

Prothrombin activity are one of the indexes to evaluate the degree of liver failure in patients.The units of this indices is %.

Observe the clinical manifestations, safety and adverse reactions of the patients

Time Frame: These indicators were collected 1 week before faecal bacteria transplantation, and change from at 5 day, 10 day, 15 day, 20 day, 4 and 8 weeks after faecal bacteria transplantation, respectively

Safety and adverse events were assessed including fever, diarrhea and elevated inflammatory markers (such as C-reactive protein and procalcitonin) before and after faecal bacteria transplantation.

Liver function change

Time Frame: Blood samples were collected 1 week before faecal bacteria transplantation, and followed up at 5 day, 10 day, 15 day, 20 day, 4 and 8 weeks after faecal bacteria transplantation, respectively

The investigators need to monitor the changes in liver and kidney function before and after faecal bacteria transplantation,such as ALT、AST、GGT 、TBIL(The units of these indices are U/L).

gut microbiota change

Time Frame: Fecal samples were collected 1 week before faecal bacteria transplantation, and change from at 5 day, 10 day, 15 day, 20 day, 4 and 8 weeks after faecal bacteria transplantation, respectively

Gene sequencing and metabonomics analysis of fecal flora.

proinflammatory cytokine change

Time Frame: Blood samples were collected 1 week before faecal bacteria transplantation, and followed up at 5 day, 10 day, 15 day, 20 day, 4 and 8 weeks after faecal bacteria transplantation, respectively

IL-17,IL-6,TNF-α, TGF-β, IFN-γ and other cytokines were detected by ELISA(The units of these indices are pg/mL).

Model for end-stage liver disease score change

Time Frame: Model for end-stage liver disease score were obtained separately in 1 week before faecal bacteria transplantation, and to access once again at 5 day, 10 day, 15 day, 20 day, 4 and 8 weeks after faecal bacteria transplantation, respectively

The model for end-stage liver disease (MELD) score is a prospectively developed and validated scale for the severity of end-stage liver disease.The higher the MELD score, the more severe the liver disease and the greater the risk of death. The fatality rate of patients with MELD between 20 and 30 was more than 30%, that of patients with MELD between 30 and 40 was more than 50%, and that of patients with MELD \>40 was more than 70%.

Study Sites (1)

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