None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The subjects included in the analysis of irrespective sex in between the age 20 years to 60 years those have no disease. The subjects are Willing to come for regular follow up visits will be included in the study.
Exclusion criteria
Exclusion criteria: The subjects having severe liver, kidney and heart diseases are excluded in the study. Patients who are currently participating in any other clinical trial. Subject with history of alcohol consumption > than 20 gm/week and/or drug abuse Known allergy, sensitivity or intolerance to the study drugs and their formulation ingredients are excluded in the study. Any condition that in the opinion of the investigator does not justify the patientââ?¬•s inclusion for the study.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome is to detect the patient condition, morbid factors, gravity of liver injury of subjects, policy for de-challenge the medication and dose if Guduchi ghana vati Induced Liver Injury will be notedTimepoint: 02 months | — |
Primary
| Measure | Time frame |
|---|---|
| The primary outcome intended to create data base of the hepatic safety and address the evidence of Guduchi ghana vati Induced Liver Injury if occurredTimepoint: 2 months | — |
Countries
India
Contacts
CCRAS, New Delhi