None listed
Conditions
Interventions
None listed
Sponsors
Centre Of Excellence scheme, Ayurswasthya Yojana, Ministry Of AYUSH, Govt of India
Eligibility
Inclusion criteria
Inclusion criteria: Apparently healthy subjects free from any known disease belonging to all gender categories in the age group of 18-60 years. Volunteers with their vitals, Hb%, Liver Function Test (LFT), Kidney Function Test (KFT), lipid profile, HbA1c values under normal range. BMI between 18.5 to 30 kg/m2 Subjects who agree to participate in the study and provide written consent.
Exclusion criteria
Exclusion criteria: Subjects under treatment for any illness. Addicted to alcohol, tobacco. Pregnant / Lactating women. Subjects who participated in any interventional clinical trial during the past three months. Other conditions which the investigator thinks may jeopardize the safety of the subject.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quantitative analysis of gallic acid absorption from Varadi ghana vati and Mustadi ghana vati in plasma samples of healthy human volunteers. Timepoint: Assessment day 1 and assessment day 2 | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of time to reach peak plasma concentration (Tmax) of gallic acid from Varadi ghana vati and Mustadi ghana vati in plasma samples of healthy human volunteers. Timepoint: Assessment day 1 and assessment day 2;Estimation of peak plasma concentration (Cmax) of gallic acid in Varadi ghana vati and Mustadi ghana vati in plasma samples of healthy human volunteers.Timepoint: Assessmnet day 1 and assessment day 2;Evaluation of area under curves estimate of gallic acid from Varadi ghana vati and Mustadi ghana vati at time 0 to t (AUC0-t) in plasma samples of healthy human volunteers.Timepoint: Assessment day 1 and assessment day 2 | — |
Countries
India
Contacts
Public ContactDr Sulochana Bhat
Central Ayurveda Research Institute, Bengaluru
Outcome results
None listed