This study is performed on healthy volunteers and drug concentration in plasma is determined..
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: General Health (Liver, Heart, and Kidney) Body Mass Index (18-28) kg/m^2 Age (18-55 years old) Informed consent
Exclusion criteria
Exclusion criteria: Nicotine consumption history Cardiovascular disease History Liver and kidney Alcohol and opioid addiction Allergy reactions history to metformin
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Drug plasma concentration. Timepoint: 0.5? 1? 1.5? 2? 2.5? 3? 3.5? 4? 4.5? 5? 6? 8? 10,12, 24 h after drug administration. Method of measurement: Liquid Chromatography Mass-Mass. | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to reach maximum plasma concentration. Timepoint: After intervention. Method of measurement: Time to reach the maximum drug concentration in plasma is recorded.;Extent of absorption. Timepoint: After intervention. Method of measurement: Calculation of area under curve of concentration -time. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences