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Status unknownNCT02899130Updated Dec 6, 2017

Effect of Polyherbal Formulation in Chronic Inactive Carriers of Hepatitis B Virus

An interventional study of Polyherbal and Placebo in Chronic Hepatitis B, sponsored by Composite Interceptive Med Science. Status unknown at 1 site in India. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-12-06.

Sponsored by Composite Interceptive Med Science · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2017), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

This trial will study the effect of a polyherbal capsule in lowering the viral load of patients with chronic Hepatitis B infection and record the incidence of from Hepatitis B surface antigen elimination in 12 months

Read the detailed description

A placebo controlled randomised trial. 3 herbs that have proven effect on eliminating the virus and normalizing liver function will be given. Equally matched placebo (blinded) will be given randomly to patients. All parameters of hepatitis B infection will be compared between the randomized groups

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Conditions studied

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In context

Hepatitis A

2,709 studies on the registry are indexed under Hepatitis A; 142 are open to participants now.

This study's planned enrollment of 80 is below the median of 100 across 1,886 interventional studies indexed under Hepatitis A.

Browse Hepatitis A studies →

Lead sponsor

Composite Interceptive Med Science is the lead sponsor of 10 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adults aged above 18 years of age, with inactive chronic hepatitis B (HB) or immune tolerant phase, with or without dyslipidaemia and having all of the following

    1. HBsAg +ve for >6 months and anti-HBs negative
    2. Alanine amino transferase ≤ 2 upper limit of normal
    3. HBeAg positive or negative irrespective of viral DNA load
    4. Not currently on antiviral therapy for Chronic hepatitis B

Exclusion criteria

Exclusion Criteria:

  • Any one of the following

    1. Patients with decompensated liver disease of any etiology(characterized by elevated bilirubin, raised International normalized ratio, or a history of ascites, variceal hemorrhage,hepatic encephalopathy, Spontaneous bacterial peritonitis, hepatorenal syndrome or Hepatocellular carcinoma)
    2. Family history of hepatocellular carcinoma
    3. Patients with HIV and Hepatitis C virus co-morbidity
    4. Pregnant, attempting to conceive, or lactating women
    5. Patients with diabetes mellitus
    6. Recent history of acute coronary syndrome (\<6months) or chronic coronary artery disease with poor left ventricular function (by physician / cardiology opinion)
    7. Patients with renal failure ( Creatinine clearance less than 60 ml/min)
    8. Active substance or alcohol abuse and concurrent use of corticosteroids or immunosuppressive agents.
    9. Presence of extra hepatic manifestations
    10. Previously treated with pegylated interferon within the last 2 years
    11. Positive fibroscan or ultrasound elastography showing evidence of fibrosis (F3 and above)
    12. Current or former employees of organic India
    13. Participating in another clinical trial with an active intervention or drug or device with last dose taken within 60 days.
    14. Refusing consent or physician uncomfortable with patient compliance to treatments or follow up.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Polyherbal

    Combination of 3 whole herbs in a capsule

    Drug: Polyherbal

  • Placebo comparator
    Matching placebo

    Similar looking inert capsules

    Drug: Placebo

Interventions

  • DrugPolyherbal

    Each capsule contains 3 herbs. Phyllanthus niruri, Boerhaavia diffusa, picrorhiza kurroa

    Also known as: Liver Kidney Care

  • DrugPlacebo

    Inactive compound that is similar looking as the intervention

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What researchers measure

Primary outcomes

  1. Number of patients with change in mean Hepatitis B Virus (HBV) DNA by at least 2log10 units from baseline at end of treatment for those with HBV DNA ≥ 1000 IU/ml.

    Time frame: 12 months

Secondary outcomes

  1. Number of patients with change in hepatitis B surface antigen titers from baseline for those with HBV DNA <1000 IU/ml

    Time frame: 12 months

  2. Number of patients with Incidence of seroconversion from Hepatitis B surface antigen to anti-Hepatitis B surface antibody

    Time frame: 12 months

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Study locations

1 of 1 sites recruiting
  • Mazumdar Shaw Mutispeciality Hospital
    Bangalore, Karnataka 560099, India
    • Alben Sigamani, MD · Principal investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 6, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02899130
Lead sponsor
Composite Interceptive Med Science
Responsible party
Sponsor
First posted
Sep 14, 2016
Start date
Oct 2016
Primary completion
Jun 2018 (estimated)
Completion
Sep 2018 (estimated)
Last update
Dec 6, 2017

Study contacts

Alben Sigamani, MD
Contact
alben.sigamani.dr@nhhospitals.org
+91 8884431444
Sanjaya Chauhan, Pharm.D
Contact
drsanjayachauhan49@gmail.com
+91 9611252350 ext. 2388
Alben Sigamani, MD
principal investigator · Narayana Hrudayalaya Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

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