Skip to content

A CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF Oâ??LIVER -T IN PATIENTS WITH HEPATITIS A VIRUS.

A PROSPECTIVE, RANDOMIZED, DOUBLE BLIND, PARALLEL GROUP, PLACEBO CONTROLLED CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF Oâ??LIVER -T IN PATIENTS WITH HEPATITIS A VIRUS.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/01/005395
Enrollment
100
Registered
2015-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: B15- Acute hepatitis A

Interventions

Intervention1: Oâ??LIVER- T (syrup): One teaspoonful three times a day, 30 minutes after Meals up to day 84 Control Intervention1: Placebo(syrup): One teaspoonful three times a day, 30 minutes after M

Sponsors

SBL PVT LTD
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Male and female subjects18- 40 years of age • Patients having acute virus A hepatitis in the serum. • Willing to provide written informed consent along with audio video visual • Subjects willing to comply with all the study procedure and requirements

Exclusion criteria

Exclusion criteria: • Who had HBsAg in the serum • Patients who had history of ingesting hepatotoxic drugs prior to the onset of symptoms. • Women with childbearing Potential and insufficient contraception. • Female who is pregnant, planning a Pregnancy (during the course of the study) or nursing a child. • Any contraindication to blood sampling. • History of HIV Positive serology.

Design outcomes

Primary

MeasureTime frame
â?¢Relief from clinical symptoms and changes of lab Parameters.Timepoint: â?¢Relief from clinical symptoms and changes of lab Parameters.

Secondary

MeasureTime frame
â?¢Incidence and rate of adverse eventsTimepoint: Screening to EOT (DAY 84)

Countries

India

Contacts

Public ContactDr Harisha S

ICBio Clinical research Pvt Ltd

harish@icbiocro.com9900111997

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026