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Intravenous BCAA for HE in ACLF (BCAA-HE-ACLF)

Primary Purpose

Hepatic Encephalopathy, Acute-On-Chronic Liver Failure

Status
Recruiting
Phase
Phase 1
Locations
India
Study Type
Interventional
Intervention
Branch Chain Amino Acid
Lactulose
Sponsored by
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatic Encephalopathy focused on measuring Hepatic Encephalopathy, Acute-On-Chronic Liver Failure, Neurological Dysfunction, Metabolomics, Systemic Inflammations, Branch Chain Amino Acid, bispectral index, Cerebral edema, Lactulose

Eligibility Criteria

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

Inclusion Criteria: Age 18-75 years Either gender Patients with ACLF (CANONIC definition) of any etiology with HE ≥grade 2 as per West-Haven Criteria Exclusion Criteria: Those who do not consent to participate in the study Patients with structural brain lesions or stroke Inability to obtain informed consent from patient or relatives Severe preexisting cardiopulmonary disease Renal dysfunction (S. Creatinine ≥ 2mg/dL) Pregnancy/Lactation Post liver transplant patients HIV infection Patients who are on psychoactive drugs, like sedatives or antidepressants Patients who are too sick to carry out the protocol.

Sites / Locations

  • Dr. Madhumita PremkumarRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experiential Arm

Comparator Arm

Arm Description

Drug: iv Branch Chain Amino Acid + Lactulose Intravenous Branched Chain Amino Acids - 500mL once daily for 3 days plus Lactulose

Drug: Lactulose + Placebo

Outcomes

Primary Outcome Measures

Improvement in survival
Survival assessment will be made by accessing all cause Mortality
Improvement in survival
Survival assessment will be made by accessing all cause Mortality
Improvement of encephalopathy by one or more grade
Improvement in scoring of hepatic Encephalopathy
Improvement of encephalopathy by one or more grade
Improvement in scoring of hepatic Encephalopathy
Dynamic Assessment of systemic inflammation (Cytokines: IL-1b, IL-6, INF-g, TNF-a, IL-15, IL-17, IL-18) at presentation and after Specific management.
Systemic inflammation will be accessed by Cytometric Bead Array
Assessment of metabolomics following BCAA + Lactulose and Lactulose alone
Metabolomics will be performed by LC/GC-MS

Secondary Outcome Measures

Reduction of arterial ammonia Level
Level of ammonia will be measured by Point of care device
Reduction of arterial ammonia Level
Level of ammonia will be measured by Point of care device
Assessment of cerebral edema
Cerebral edema will be assessed by Magnetic Resonance Imaging+ Magnetic Resonance Spectroscopy
Prevention/reduction of cerebral edema based on optic nerve sheath diameter (ONSD)
ONSD measurement will be done by Ultrasound
Reduction of consciousness recovery time among survivors
Consciousness will be assessed by cognitive battery tests

Full Information

First Posted
December 6, 2022
Last Updated
January 17, 2023
Sponsor
Postgraduate Institute of Medical Education and Research
Collaborators
Amrita Institute of Medical Sciences & Research Center, Asian Institute of Gastroenterology, India, All India Institute of Medical Sciences, Bhubaneswar, Kalinga Institute of Medical Sciences, Bhubaneswar
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1. Study Identification

Unique Protocol Identification Number
NCT05700695
Brief Title
Intravenous BCAA for HE in ACLF (BCAA-HE-ACLF)
Official Title
Intravenous Branched-chain Amino Acids for Overt Hepatic Encephalopathy in Patients With Acute on Chronic Liver Failure - A Multi-centric Double-blind Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 17, 2023 (Actual)
Primary Completion Date
April 25, 2025 (Anticipated)
Study Completion Date
April 25, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research
Collaborators
Amrita Institute of Medical Sciences & Research Center, Asian Institute of Gastroenterology, India, All India Institute of Medical Sciences, Bhubaneswar, Kalinga Institute of Medical Sciences, Bhubaneswar

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This multi-centric study analyses the effect of intravenous branched-chain amino acids (BCAA) on overt HE in patients with ACLF. The investigators aim to study the efficacy of combining intravenous BCAA with lactulose versus lactulose alone, ammonia measures, endotoxin, metabolomics, and cerebral edema in the medical management of overt HE in patients with ACLF. The study will also access the impact on overall survival and improvement in the grade of HE.
Detailed Description
Treatment of HE in ACLF is based on extrapolation of data available from cirrhotic patients with HE. The mainstay of treatment remains Lactulose. Rifaximin is added on to therapy who have a breakthrough episode of HE on lactulose. BCAA is used as an add-on therapy if patients have minimal/covert encephalopathy, are protein intolerant or have recurrent HE. No studies are available assessing the adjuvant effect of intravenous BCAA on ammonia reduction in HE in patients with ACLF. So, this study has been designed to analyze the effect of intravenous BCAA on hepatic encephalopathy in patients with ACLF. This study will also analyze the systemic and neuronal inflammation, metabolomics, and cerebral edema under the effect of intravenous BCAA in HE patients with ACLF.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatic Encephalopathy, Acute-On-Chronic Liver Failure
Keywords
Hepatic Encephalopathy, Acute-On-Chronic Liver Failure, Neurological Dysfunction, Metabolomics, Systemic Inflammations, Branch Chain Amino Acid, bispectral index, Cerebral edema, Lactulose

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Prospective interventional cohort study
Masking
Investigator
Masking Description
Double-blind
Allocation
Randomized
Enrollment
246 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experiential Arm
Arm Type
Experimental
Arm Description
Drug: iv Branch Chain Amino Acid + Lactulose Intravenous Branched Chain Amino Acids - 500mL once daily for 3 days plus Lactulose
Arm Title
Comparator Arm
Arm Type
Active Comparator
Arm Description
Drug: Lactulose + Placebo
Intervention Type
Drug
Intervention Name(s)
Branch Chain Amino Acid
Intervention Description
Intravenous branched chain amino acids will be given for 3 days to patients in experimental arm
Intervention Type
Drug
Intervention Name(s)
Lactulose
Intervention Description
Oral lactulose will be given to patients in both arms
Primary Outcome Measure Information:
Title
Improvement in survival
Description
Survival assessment will be made by accessing all cause Mortality
Time Frame
Day 7
Title
Improvement in survival
Description
Survival assessment will be made by accessing all cause Mortality
Time Frame
Day 28
Title
Improvement of encephalopathy by one or more grade
Description
Improvement in scoring of hepatic Encephalopathy
Time Frame
Day 3
Title
Improvement of encephalopathy by one or more grade
Description
Improvement in scoring of hepatic Encephalopathy
Time Frame
Day 7
Title
Dynamic Assessment of systemic inflammation (Cytokines: IL-1b, IL-6, INF-g, TNF-a, IL-15, IL-17, IL-18) at presentation and after Specific management.
Description
Systemic inflammation will be accessed by Cytometric Bead Array
Time Frame
Day 0
Title
Assessment of metabolomics following BCAA + Lactulose and Lactulose alone
Description
Metabolomics will be performed by LC/GC-MS
Time Frame
Day 7
Secondary Outcome Measure Information:
Title
Reduction of arterial ammonia Level
Description
Level of ammonia will be measured by Point of care device
Time Frame
Day 3
Title
Reduction of arterial ammonia Level
Description
Level of ammonia will be measured by Point of care device
Time Frame
Day 7
Title
Assessment of cerebral edema
Description
Cerebral edema will be assessed by Magnetic Resonance Imaging+ Magnetic Resonance Spectroscopy
Time Frame
Discharge form Hospital and 3 month of episode of HE
Title
Prevention/reduction of cerebral edema based on optic nerve sheath diameter (ONSD)
Description
ONSD measurement will be done by Ultrasound
Time Frame
72 Hours
Title
Reduction of consciousness recovery time among survivors
Description
Consciousness will be assessed by cognitive battery tests
Time Frame
30 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: Age 18-75 years Either gender Patients with ACLF (CANONIC definition) of any etiology with HE ≥grade 2 as per West-Haven Criteria Exclusion Criteria: Those who do not consent to participate in the study Patients with structural brain lesions or stroke Inability to obtain informed consent from patient or relatives Severe preexisting cardiopulmonary disease Renal dysfunction (S. Creatinine ≥ 2mg/dL) Pregnancy/Lactation Post liver transplant patients HIV infection Patients who are on psychoactive drugs, like sedatives or antidepressants Patients who are too sick to carry out the protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Madhumita Premkumar, DM
Phone
7087003409
Email
drmadhumitap@gmail.com
Facility Information:
Facility Name
Dr. Madhumita Premkumar
City
Chandigarh
ZIP/Postal Code
160012
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr. Madhumita Premkumar, MD
Phone
+919540951061
Email
drmadhumitap@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21163546
Citation
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Citation
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Citation
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Citation
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
Rossi-Fanelli F, Riggio O, Cangiano C, Cascino A, De Conciliis D, Merli M, Stortoni M, Giunchi G. Branched-chain amino acids vs lactulose in the treatment of hepatic coma: a controlled study. Dig Dis Sci. 1982 Oct;27(10):929-35. doi: 10.1007/BF01316578.
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PubMed Identifier
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Citation
Cordoba J, Ventura-Cots M, Simon-Talero M, Amoros A, Pavesi M, Vilstrup H, Angeli P, Domenicali M, Gines P, Bernardi M, Arroyo V; CANONIC Study Investigators of EASL-CLIF Consortium. Characteristics, risk factors, and mortality of cirrhotic patients hospitalized for hepatic encephalopathy with and without acute-on-chronic liver failure (ACLF). J Hepatol. 2014 Feb;60(2):275-81. doi: 10.1016/j.jhep.2013.10.004. Epub 2013 Oct 12.
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Dam G, Aamann L, Vistrup H, Gluud LL. The role of Branched Chain Amino Acids in the treatment of hepatic Encephalopathy. J Clin Exp Hepatol. 2018 Dec;8(4):448-451. doi: 10.1016/j.jceh.2018.06.004. Epub 2018 Jun 27.
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Intravenous BCAA for HE in ACLF (BCAA-HE-ACLF)

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