Skip to content

Efficacy of Addition of Fecal Microbiota Transplant (FMT) and Plasma Exchange to Tenofovir in Comparison to Monotherapy With Tenofovir in ACLF-HBV

Efficacy of Addition of Fecal Microbiota Transplant (FMT) and Plasma Exchange to Tenofovir in Comparison to Monotherapy With Tenofovir in ACLF-HBV

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04431375
Enrollment
70
Registered
2020-06-16
Start date
2020-06-22
Completion date
2022-06-10
Last updated
2022-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute-On-Chronic Liver Failure, Hepatitis B

Brief summary

A randomized controlled trial to study the efficacy of addition of FMT & plasma exchange to tenofovir compared to monotherapy with tenofovir in patients with HBV reactivation who develops Acute on chronic liver failure. In this study the patients who meet the inclusion criteria will be randomized to either receive Tenofovir or with FMT + plasma exchange along with Tenofovir . Blood samples & stool samples will be taken & analysis will be done accordingly .The patients are followed for 90 days MELD,APACHE & SOFA scores are calculated.Then statistical analysis will be done to find whether the addition of plasma exchange & FMT adds benefit compared to tenofovir treatment alone .

Detailed description

A randomized controlled trial to study the efficacy of addition of FMT & plasma exchange to tenofovir compared to monotherapy with tenofovir in patients with HBV reactivation who develops Acute on chronic liver failure. In this study the patients who meet the inclusion criteria will be randomized to either receive Tenofovir or with FMT + plasma exchange along with Tenofovir . Blood samples & stool samples will be taken & analysis will be done accordingly .The patients are followed for 90 days MELD,APACHE & SOFA scores are calculated.Then statistical analysis will be done to find whether the addition of plasma exchange & FMT adds benefit compared to tenofovir treatment alone . Study period: 2 Years Intervention: The patients in Group A will receive T.Tenofovir \[antiviral\] 300mg per oral once a day . The patients in Group B will receive Plasma exchange 2 sessions alternate day followed by FMT for 7 days and Tenofovir \[antiviral\] 300mg PO once a day . Intravenous antibiotics will be given to all patients included in study empirically, because of high risk of infection in these patients. Patients with sepsis are excluded from the study. Methodology for FMT - Fresh Stool \[30 g\] is obtained from donor \<3 hr before FMT. 150 mL sterile 0.9N saline is added to sample & homogenized in a blender. It is Continued 3 times in pulses of 20-30 secs, till homogenous suspension. Slow filtration is done with membrane filter (330µm) to give adequate time. Filtration is repeated 3 times. Patient is kept NPO for 4 hrs. prior to the instillation .100 ml of fresh filtrate is given for 7 days through naso-jejunal tube over 5-10 minutes .Patient is kept reclined at 45° for 4 hr. Normal diet is given after 2 hr of procedure. IV antibiotics are continued as per institutional protocol in case of sepsis. Methodology for plasma exchange \[PE\] - Circulatory access will be established through a double lumen catheter via the patient's femoral vein. The total exchanged plasma volume will be 2500-3500 mL, and the Plasma Exchange rate will be 20-25 mL/min. Fresh-frozen plasma (FFP) will be supplied by the ILBS Blood Bank. Dexamethasone (5 mg) and heparin (2500 U) will be injected routinely before PE. Heparin will be neutralized at the end of PE by an injection of 20-50 mg protamine sulfate. PE will be repeated alternate day for a total of 2 sessions Adverse effects: FMT FMT - Sore throat and difficulty in deglutition secondary to naso-gastric tube insertion Plasma exchange PE * Hypocalcemia * Hypokalemia * Metabolic alkalosis * Hypotension * Anaphylaxis * TRALI TENOFOVIR Tenofovir * Reversible proximal renal tubular toxicity. * Reduced bone mineral density * Manifestations of mitochondrial toxicity (i.e., neuropathy, myopathy, lactic acidosis Stopping rule of study: * Allergic reactions except mild drug reactions * Arterial hypotension or development of shock /Hypertension * Arrhythmias * Development or progression of organ failures during therapy * Transfusion related lung injury * Uncontrolled Bleeding or DIC * Severe dyselectrolytemia( k+\<2.5 or \>5.5) * Seizures/tetany * Patients who are undergoing or listed for Transplantation

Interventions

BIOLOGICALPlasma Exchange

Plasma exchange 2 sessions alternate day followed by FMT for 7 days and Tenofovir \[antiviral\] 300mg PO once a day .

DRUGTenofovir

Tenofovir \[antiviral\] 300mg PO once a day .

OTHERFecal Mircobiota Transplantation

FMT for 7 days

Sponsors

Institute of Liver and Biliary Sciences, India
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age - 18-75 years * Patients with ACLF - HBV reactivation according to APASL guidelines. * MELD \< 30 WITH AKI,HE * MELD \< 30 WITH OUT EXTRAHEPATIC FAILURE

Exclusion criteria

* MELD \> 30 * Co existing hepatitis A,E,D * HCC * Sepsis * Alcohol intake, substance abuse, HIV, IBD, chronic constipation or diarrhoea * Allergy to plasma, protamine or heparin, * Active hemorrhage or disseminated intravascular coagulation (DIC) * Unstable hemodynamics (e.g., blood pressure \<90/60 mmHg, heart rate \>100 bpm), * Cerebral or myocardiac infarction * Pregnancy

Design outcomes

Primary

MeasureTime frame
Overall survival in both groupsDay 28

Secondary

MeasureTime frameDescription
Reduction in HBV DNA level14 days
Reduction in CTP Score in both groups14 daysCTP Score ranges from 5 to 15 5=good 15=worst
Reduction in MELD Score in both groups14 daysMELD Score ranges from 6 to 40 6=good 40=worst
Percentage of patient's with improvement in hepatic failure calculated by MELD Na and CTP scores.14 days
Percentage of patient's with improvement in hepatic failure calculated by MELD Na30 days
Overall survival in both groups3 months
Percentage of patient's with improvement in hepatic failure calculated by MELD Na.90 days
Change in microbiota profile in both groups10 days
Change in plasma cytokine profile in both groups10 days
Number of patients with adverse Events in both groups90 days
Percentage of patient's with improvement in hepatic failure calculated by CTP scores.30 days

Countries

India

Contacts

Primary ContactDr G. Srinivasa Reddy, MD
srinivasareddygolamari@gmail.com01146300000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026