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Plasma Exchange in Acute on Chronic Liver Failure (PLEXAR)

Primary Purpose

Cirrhosis, Liver, Acute-On-Chronic Liver Failure

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Plasma exchange
Standard medical treatment
Sponsored by
Asian Institute of Gastroenterology, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis, Liver focused on measuring Plasma exchange, Acute on chronic liver failure

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed with ACLF as per APASL criteria with AARC score of ≥8

Exclusion Criteria:

  1. Uncontrolled sepsis
  2. Septic shock requiring inotropes despite fluid resuscitation
  3. Active or recent bleeding (unless controlled for >48 hours).
  4. Severe thrombocytopenia (≤20×10^9/L)
  5. Acute kidney injury with Creatinine > 2 or the need of RRT
  6. Respiratory failure (Severe ARDS)
  7. Chronic kidney disease
  8. Hepatocellular carcinoma outside Milan criteria (1 nodule ≤5 cm or 3 nodules ≤3 cm)
  9. HIV infection
  10. Pregnancy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Plasma exchange

    Standard medical treatment

    Arm Description

    The consented patients will receive standard medical management with sessions of single volume plasma exchange with fresh frozen plasma and 5% human albumin.Plasma exchange session will be done on an alternate day to a maximum of 5 procedures.

    The consented patients will receive standard medical treatment which includes adequate nutrition (35-45 Kcal/Kg with 1.5gm/Kg protein) diuretics, anti HE measures, appropriate antibiotics for infections, entecavir 0.5 mg once daily for hepatitis B, and steroids for autoimmune hepatitis.

    Outcomes

    Primary Outcome Measures

    Overall Survival

    Secondary Outcome Measures

    Transplant free survival
    Development of organ dysfunction
    Development of cirrhosis complications
    Improvement in Model for end stage liver disease score

    Full Information

    First Posted
    August 3, 2019
    Last Updated
    August 8, 2019
    Sponsor
    Asian Institute of Gastroenterology, India
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04051437
    Brief Title
    Plasma Exchange in Acute on Chronic Liver Failure
    Acronym
    PLEXAR
    Official Title
    Therapeutic Plasma Exchange in Patients With Acute on Chronic Liver Failure: A Randomized Controlled Trial (PLEXAR)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 15, 2019 (Anticipated)
    Primary Completion Date
    March 31, 2020 (Anticipated)
    Study Completion Date
    March 31, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Asian Institute of Gastroenterology, India

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Acute on chronic liver failure (ACLF) is a distinct syndrome in patients with chronic liver disease with rapid clinical deterioration and has high short term mortality within one month.Despite aggressive clinical care, only half of the patients could survive an episode of ACLF. The investigators hypothesized that the early treatment with therapeutic plasma exchange with plasma and albumin in ACLF patients might improve overall survival in carefully selected patients by removing cytokines, chemokines and toxic substances.
    Detailed Description
    Acute on chronic liver failure (ACLF) lacks a consensus definition and definitive management approaches. The various management strategies include treatment of acute insult, support of multiple organ systems and disease-specific medications such as antivirals for hepatitis B, steroids for alcoholic hepatitis, and autoimmune hepatitis. Despite aggressive clinical care, only half of the patients could survive an episode of ACLF. ACLF is a dynamic condition and has specific time-related disease course. Majority of patients of the patients attain their final grade of ACLF between 3 rd and 7th day and makes it an ideal time to assess the prognosis. Recently, liver transplantation option also explored in patients not responding to standard medical care and appeared promising. Early liver transplantation is considered if the baseline model for end-stage liver disease (MELD) score > 28, Asia pacific association for the study of the liver (APASL) ACLF Research Consortium (AARC) score of > 10, advanced hepatic encephalopathy in the absence of organ failures or overt sepsis. However, liver transplantation is feasible only in 25% cases and approximately 67% waitlist mortality. Treating ACLF patients early in the disease course, i.e., window period, may prevent multiorgan dysfunction and improve outcomes. Therefore, these alternative modalities can act as bridging to liver transplantation and hasten the spontaneous liver regeneration and hence, transplant-free recovery in some patients. Plasma exchange has been shown to reduce cytokines, inflammatory mediators, and damage-associated molecular patterns. The early experience of therapeutic plasma exchange in patients with hepatitis B ACLF shows a survival benefit compared to standard of care. Changes in albumin quantity and quality are noted in patients with cirrhosis. An increase in oxidized albumin, ischemia-modified albumin, and albumin dimerization is observed ACLF patients and changes are more pronounced compared to cirrhotic patients. These changes are well correlated with short and long term mortality. Hence the investigators hypothesized that the early treatment with therapeutic plasma exchange with plasma and albumin in ACLF patients improves overall survival in carefully selected patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cirrhosis, Liver, Acute-On-Chronic Liver Failure
    Keywords
    Plasma exchange, Acute on chronic liver failure

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    130 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Plasma exchange
    Arm Type
    Experimental
    Arm Description
    The consented patients will receive standard medical management with sessions of single volume plasma exchange with fresh frozen plasma and 5% human albumin.Plasma exchange session will be done on an alternate day to a maximum of 5 procedures.
    Arm Title
    Standard medical treatment
    Arm Type
    Active Comparator
    Arm Description
    The consented patients will receive standard medical treatment which includes adequate nutrition (35-45 Kcal/Kg with 1.5gm/Kg protein) diuretics, anti HE measures, appropriate antibiotics for infections, entecavir 0.5 mg once daily for hepatitis B, and steroids for autoimmune hepatitis.
    Intervention Type
    Procedure
    Intervention Name(s)
    Plasma exchange
    Intervention Description
    During each plasma exchange session 3-4lt (1.2-1.3 times of plasma volume) of plasma will be exchanged with fresh frozen plasma and 5% albumin. Plasma exchange session will be done on an alternate day to a maximum of 5 procedures. PLEX will be discontinued if the patients Shows sustained clinical improvement, Receive liver transplantation, Refuses further PLEX session No improvement in clinical condition Intolerant to PLEX procedure
    Intervention Type
    Drug
    Intervention Name(s)
    Standard medical treatment
    Intervention Description
    The consented patients will receive standard medical treatment which includes adequate nutrition (35-45 Kcal/Kg with 1.5gm/Kg protein) diuretics, anti HE measures, appropriate antibiotics for infections,tablet entecavir 0.5 mg once daily for hepatitis B, and steroids for autoimmune hepatitis.
    Primary Outcome Measure Information:
    Title
    Overall Survival
    Time Frame
    90 days
    Secondary Outcome Measure Information:
    Title
    Transplant free survival
    Time Frame
    90 days
    Title
    Development of organ dysfunction
    Time Frame
    28 days
    Title
    Development of cirrhosis complications
    Time Frame
    28 days
    Title
    Improvement in Model for end stage liver disease score
    Time Frame
    90 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients diagnosed with ACLF as per APASL criteria with AARC score of ≥8 Exclusion Criteria: Uncontrolled sepsis Septic shock requiring inotropes despite fluid resuscitation Active or recent bleeding (unless controlled for >48 hours). Severe thrombocytopenia (≤20×10^9/L) Acute kidney injury with Creatinine > 2 or the need of RRT Respiratory failure (Severe ARDS) Chronic kidney disease Hepatocellular carcinoma outside Milan criteria (1 nodule ≤5 cm or 3 nodules ≤3 cm) HIV infection Pregnancy
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Pramod Kumar, MD
    Phone
    +91-9814933544
    Email
    dapramod@gmail.com

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Plasma Exchange in Acute on Chronic Liver Failure

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