Skip to content

Study on Fatty liver disease in Unani Medicine

Efficacy of Arq Biranjasif in the secondary prevention of fatty liver disease and its risk factors with associated conditions. - FLD

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/069842
Enrollment
41
Registered
2024-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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: Arq Biranjasif: 120ml/day (60ml BD) will be provided in two divided doses. Control Intervention1: Arq Biranjasif: 120ml/day (60ml BD) will be provided in two divided doses. Control Inte

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subjects of all gender, age of 19 to 75 years. 2.Diagnosed fatty liver disease on the basis of USG abdomen within one month or diagnosed during screening. 3.Either subjects with obesity (those who are not taking medication for obesity) or subjects with type-II diabetes mellitus or both. 4.Subjects willing to participate.

Exclusion criteria

Exclusion criteria: 1.Pregnancy or lactating mothers. 2.Subjects with hangover sickness. 3.Boozer subjects (alcohol consumption of more than 14 drinks per week (men) and more than 7drinks per week (women) 4.Subjects consuming hypolipidemic and anti- inflammatory drugs. 5.Subjects in any treatment known to affect hepatic function. 6.History of renal diseases, cardiovascular diseases, pulmonary diseases. 7.Subjects with total parenteral nutrition or bedridden subjects. 8.Subjects with protein malnutrition 9.Subjects with type 2 DM on insulin treatment. 10.Subjects with jejunoileal bypass surgery. 11.Patients on the following drugs and toxins - amiodarone, coralgil, tamoxifen, perhexiline maleate, corticosteroids, synthetic estrogens, methotrexate, iv tetracycline, highly active antiretroviral drugs (HAART).

Design outcomes

Primary

MeasureTime frame
Improvement in investigational valuesTimepoint: Intervention Period 8 weeks, Enrollment period 1 year

Secondary

MeasureTime frame
Not ApplicableTimepoint: not Applicable

Countries

India

Contacts

Public ContactDr C Raziya Thaseen

National Institute of Unani Medicine

Arish_sherwani@yahoo.co.in9448794691

Outcome results

None listed

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