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Homoeopathic treatment of fatty liver

Repertorial approach of treating non-alcoholic fatty liver disease in adults using individualized homoeopathic medicines: A single-arm, pre-post trial

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050323
Enrollment
60
Registered
2023-03-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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 homeopathic medicines in centesimal potencies: Intervention is planned as administering indicated homoeopathic medicines in centesimal potencies (CH). Each dose will cons
dosage and repetition depending upon the individual requirement of the cases. Patients will be advised to refrain from handling the globules or from eating, drinking, smoking or brushing teeth within

Sponsors

D N De Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient with grade I and II NAFLD established by ultrasound and altered liver enzyme (serum ALT level >=40 IU/L) [ICD-10 code: K 76.0]. 2. Age between 18 and 65 years. 3. Participants of either sex and transgender. 4. Literate patients; ability to read English and/or Bengali and/or Hindi; Illiterate people will be interviewed by the investigators maintaining adequate privacy to fill up the questionnaires. 5. Providing with written informed consent voluntarily to participate.

Exclusion criteria

Exclusion criteria: 1. Regular or excessive use of alcohol and any other addiction. 2. History of chronic liver disease (Viral hepatitis B or C, autoimmune hepatitis). 3. Cholestatic and metabolic liver diseases, hepatic steatosis., hemochromatosis and liver transplants. 4. Combined with uncontrolled diabetes, uncontrolled hypertension, uncontrolled hypothyroidism, kidney or heart disease, stroke or any other severe systemic diseases affecting quality of life. 5. Person under corticosteroid therapy, substance abuse. 6. Vulnerable population â?? unconscious, non-ambulatory, too sick for consultation, differently abled, terminally ill or critically ill, mentally incompetent people. 7. Pregnant and puerperal women and lactating mother. 8. Self-reported immune-compromised state. 9. Already undergoing homoeopathic treatment within last 3 months for any other disease. 10. Simultaneous participation in any other trials.

Design outcomes

Primary

MeasureTime frame
Serum ALT levelTimepoint: At baseline and after 3 months

Secondary

MeasureTime frame
Blood Lipid ProfileTimepoint: At baseline and after 3 months;Chronic Liver Disease Questionnaire (CLDQ)Timepoint: At baseline, and every month, up to 3 months of intervention;Measure Yourself Medical Outcome Profile v2 (MYMOP-2) questionnaireTimepoint: At baseline, and every month, up to 3 months of intervention;Serum AST levelTimepoint: At baseline and after 3 months;USG featuresTimepoint: At baseline and after 3 months

Countries

India

Contacts

Public ContactSanjib Sarkar

D N De Homoeopathic Medical College and Hospital

sanjibsarkar1102@gmail.com9903701819

Outcome results

None listed

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