None listed
Conditions
Interventions
Intervention 1: Intervention group 1: Oral administration of a single dose of 75 g of sugar to healthy volunteers under fasting conditions in the morning of the experiment day. Intervention 2: Interve
Sponsors
Fatak Chemie Pars Pharmaceuticals
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: 18-55 years of age. The subject is able and willing to provide signed informed consent. The subject is available for the entire study period. Willing to adhere to protocol requirements as evidenced by written informed consent. The subject has a stable residence and telephone. Good health as determined by lack of clinically significant abnormalities in health assessments performed at screening.
Exclusion criteria
Exclusion criteria: History of allergy or sensitivity to acarbose. History of any drug hypersensitivity or intolerance which, in the opinion of the investigator,would compromise the safety of the subject of the study. Significant history or current evidence of chronic infectious disease, system disorder or organ dysfunction. Presence of gastrointestinal disease or history of malabsorption within the last year. History of a medical disorders occurring within the last year that required hospitalization or medication. Use of pharmacologic agents known to significantly induce or inhibit drug-metabolizing enzymes within 30 days prior to dosing. Receipt of any drug as part of a research study within 30 days prior to the present study. Donation or significant loss of whole blood (480 ml or more) within 30 days prior to the present study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plasma glucose concentration. Timepoint: At time -15, 0, 10, 20, 30, 40, 50, 60 minutes, and then 1.25, 1.5, 2, 2.5, 3, 3.5 and 4 hours after drug administratio. Method of measurement: Blood sampling and measurement of plasma glucose concentrations.;Area under plasma glucose concentration-time curve. Timepoint: At time -15, 0, 10, 20, 30, 40, 50, 60 minutes, and then 1.25, 1.5, 2, 2.5, 3, 3.5 and 4 hours after drug administratio. Method of measurement: Blood sampling and measurement of plasma glucose concentrations. | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to reach maximum plasma glucose concentration. Timepoint: By selecting highest plasma glucose concentrations at time -15, 0, 10, 20, 30, 40, 50, 60 minutes after drug administration. Method of measurement: Blood sampling and measurement of plasma glucose. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHossein Amini
Gorgan University of Medical Sciences
Outcome results
None listed