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Efficacy of Liv Shuddhi Tablets for Non Alcoholic Fatty Liver

An Open Label Single Arm Clinical Study to Evaluate the Efficacy of Liv Shuddhi Tablets in Patients Having Non Alcoholic Fatty Liver - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/05/087609
Enrollment
60
Registered
2025-05-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: K760- Fatty (change of) liver, not elsewhere classified

Interventions

Intervention1: Liv Shuddhi Tablets: Test Product: Liv Shuddhi Tablets Dose: 1 tablet TID Route of Administration: Oral Duration: 30 Days Control Intervention1: Not Applicable: Not Applicable

Sponsors

Jeena Sikho Lifecare Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subject from 18 to 65 years of age. Subject having SGPT range above 56 unit per litre Subjects that are able to give written informed consent in a manner approved by the institutional ethics committee and comply with the requirements of the study. Subject willing to avoid participation in any other interventional clinical trial for the duration of the study.

Exclusion criteria

Exclusion criteria: Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e., biologics), including oral or parenteral corticosteroids. Subject having SGPT above 300unit/litre should exclude from the study. Subjects that have participated in any other interventional clinical trial in the previous 90 days. Subjects with known sensitivity to any of the constituents of the investigational product. Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures. Chronic illness which may influence the outcome of the study. Pregnant/nursing mothers

Design outcomes

Primary

MeasureTime frame
1. Change in LFT profile 2. Change in KFT(Kidney Function Test) profile 3. Change in Lipid Profile 4. Change CBC parameters 5. Change in Subject Global Assessment Timepoint: At T+1day, T+30days

Secondary

MeasureTime frame
Not ApplicableTimepoint: Not Applicable

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org8937015757

Outcome results

None listed

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