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Homoeopathic Medicine for Fatty Liver

Efficacy of Individualized Homoeopathic Medicines in The Treatment of Grade-1 Non-Alcoholic Fatty Liver Disease: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056609
Enrollment
140
Registered
2023-08-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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: Individualized Homoeopathic medicines in centesimal potencies with lifestyle modification: Intervention is planned as administering indicated homoeopathic remedies in centesimal potenc
dosage and repetition depending upon the individual requirement of the cases. All medicines will be procured from a Good Manufacturing Practice (GMP)- certified firm. Along with medicine interventio
dosage and repetition depending upon the individual requirement of the cases. Along with placebo comparator arm will also receive lifestyle modifications. Duration of therapy 6 months.

Sponsors

The Calcutta Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Cases attending OPD with ultra-sonographic evidence of grade-1 fatty liver. 2. Literate patients; ability to read and write in Bengali, Hindi, and/or English. 3. Patients giving written informed consent

Exclusion criteria

Exclusion criteria: 1.Cases too sick for consultation. 2. Patient unwilling to take part or not giving consent to join the study. 3. Diagnosed cases of viral hepatitis, Wilson disease, hemochromatosis, celiac disease, liver cirrhosis, hepatocellular carcinoma or any other malignancies or any uncontrolled systemic diseases, unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure. 4. Cases with history of usage of some drugs (e.g., amiodarone, corticosteroids, methotrexate, tamoxifen, synthetic estrogens, valproic acid, intravenous tetracycline, and highly active antiretroviral drugs) 5. Self-reported immune compromised state. 6. Alcohol or any other substance abuse and/or dependence. 7. Pregnant and lactating women. 8. Patient simultaneously taking part in other clinical trial in the same institute.

Design outcomes

Primary

MeasureTime frame
UltrasonographyTimepoint: at baseline & after 6 months

Secondary

MeasureTime frame
EQ-5D-5L QuestionnaireTimepoint: at baseline, after 3 months & after 6 months;Lipid profileTimepoint: at baseline, after 3 months & after 6 months;Liver function testTimepoint: at baseline, after 3 months & after 6 months

Countries

India

Contacts

Public ContactProf Dr Himangsu Hait

The Calcutta Homoeopathic Medical College and Hospital

haitdrhimangsu@gmail.com9433565680

Outcome results

None listed

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