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Clinical Trials/CTRI/2022/07/044203
CTRI/2022/07/044203
Recruiting
Phase 3

A Prospective, Randomized, Double-Blind, Two-Arm, Placebo-Controlled Comparative Clinical Study to Evaluate the Safety and Efficacy of Liv.52 Tablets in Alcoholic Liver Disease

Himalaya Wellness Company0 sites0 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Himalaya Wellness Company
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Patients of either gender aged \>18 to \<65 years.
  • 2\.Patients diagnosed as Alcoholic Liver Disease (ALD) ? on the basis of all of the following criteria:
  • a.Patient with a history of alcohol use based on AUDIT (Alcohol Use Disorders Inventory Test) questionnaire (A total sum of \>8 for men and \>4 for women)
  • b.Ongoing consumption of Alcohol or Active alcohol use until 4 weeks prior to screening.
  • c.Patients with elevated liver function test (ALT and AST \>1\.5 times of upper limit of normal (ULN) \& GGT \> 2\.5 ULN)
  • d.Ultrasound evidence of fatty liver (steatosis) and / Hepatitis.
  • e.Maddrey Discriminant function (DF) less than 32\.
  • 3\.Patient has not participated in a similar investigation in past four weeks.
  • 4\.Presenting with one or more clinical symptoms of Alcoholic liver disease like nausea, loss of appetite, jaundice, fatigue, abdominal discomfort, increased thirst, swelling, weight loss (due to loss of proximal muscle mass), weakness, mood swings, bleeding gums, dysphagia, Weight gain (due to ascites), confusion, amenorrhea etc
  • 5\.Ability to understand and willing to give a written informed consent prior to any study\-related procedures and ready to follow and in agreement to visits as per the study assessment visits

Exclusion Criteria

  • 1\.Severe alcoholic hepatitis with cirrhosis or any of its complications (e.g., Hepatocellular Carcinoma, Portal hypertension, uncontrolled infection, Acute Kidney Injury etc.)
  • 2\.Patient with other cause of Chronic Liver Disease (Nonalcoholic fatty liver disease (NAFLD), Autoimmune Liver Disease, Wilson Disease, Viral Hepatitis (HBV, HCV), hemochromatosis) and metabolic syndrome
  • 3\.Hepatic disorders due to cardiac causes, inherited metabolic causes.
  • 4\.Participants with active viral hepatitis.
  • 5\.Undergoing active treatment for alcohol withdrawal syndrome (AWS) at the study entry.
  • 6\.Participants on hepatotoxic medications like antitubercular medication, antiviral medication.
  • 7\.Severe cases of ascites, (however, Grade I \& II as per CTCAE criteria can be enrolled.) hepatic encephalopathy, varices, or bleeding.
  • 8\.Subjects with elevated liver function test ALT and AST \> 5 times of upper limit of normal (ULN)
  • 9\. Patients are on treatment for AUD (Alcohol Use Disorder)
  • 10\. Pregnant or lactating women or who don’t want to follow the effective contraception measures.

Outcomes

Primary Outcomes

Not specified

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