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A clinical trial to study the effects of the drug capsule dabeedul ward in patients with non alcoholic fatty liver disease

Evaluation Of Efficacy Of Majoon Dabeedul Ward(Sugarfree) In the management of NAFLD using quantitative fat measurement by Shearwarve Imaging - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059554
Enrollment
40
Registered
2023-11-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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: Majoon Dabeedulward (Sugarfree): Majoon Dabeedul ward (Sugarfree) in 500mg capsule form to be taken orally twice daily Control Intervention1: Placebo: A Placebo (powdered form) 500mg ro

Sponsors

Jamia Hamdard
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18-60 years Patient of all genders Patient willing to participate and sign the written informed consent Patient diagnosed as having fatty liver based on the ultrasonography report Patients with/ without clinical signs and symptoms

Exclusion criteria

Exclusion criteria: Age below 18 and above 60 years Use of alcohol or any other drug abuse Patients diagnosed with any coexisting liver disease Pregnant and lactating women Patients suffering with Hypertension, CKD, CAD, CLD or uncontrolled DM,thyroid disorder. Patient having immune-compromised status. Patient using lipid lowering drugs or dietary supplements within the last 3 weeks. Oral contraceptives & corticosteroids. Neurological disorders like epilepsy or psychiatric disorders Patient having history of Pancreatitis

Design outcomes

Primary

MeasureTime frame
Abdominal ultrasound - We will assess steatotic liver changes by Quantitative Tissue attenuation measurement with S-Shearwave Imaging Technique before and after drug administrationTimepoint: From baseline to 12 weeks

Secondary

MeasureTime frame
1)Lipid profile Change in lipid profile (Total Cholesterol, HDL,LDL,Triglycerides, VLDL) after therapy (if any) 2)Levels of Alanine transaminase (ALT) - Changes in Alanine transaminase units per litre after therapy (if any) 3)Levels of Aspartate transaminase (AST) - Changes in Aspartate transaminase (AST)units per litre after therapy (if any) 4)Levels of Alkaline phosphatase(ALP) - Changes in Alkaline phosphatase (ALP) in IU after therapy (if any) 5)Levels of Albumin and total protein- Changes in Albumin and total protein in gm/L after therapy (if any) 6) Levels of Bilirubin- Changes in Bilirubin in µmol/L after therapy (if any) 7)Levels of total protein - Changes in total protein in gm/L after therapy (if any) 8)Levels of Gammaglutamyltra nsferase(GGT)- Changes in Gamma-glutamyltransferase (GGT) units per liter after therapy (if any ) 9)Levels of lactate dehydrogenase (LDH)- Changes in L-lactate dehydrogenase (LDH) units per liter after therapyTimepoint: 12 weeks

Countries

India

Contacts

Public ContactAzhar Jabin

Jamia Hamdard

ajabin@jamiahamdard.ac.in9899315252

Outcome results

None listed

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