The objective of the study is to compare the pharmacokinetics and pharmacodynamics of a new sublingual formulation of aspirin with that of oral aspirin when administered to healthy volunteers under fasting conditions. The test product is sublingual aspirin 80 mg manufactured by Vita Green Health Products Co. Ltd, Hong Kong and the reference product is oral aspirin 80mg tablet manufactured by Synco (HK) Ltd, Hong Kong.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Vita Green Health Products sublingual aspirin 80 mg tablet
Synco (HK) oral aspirin 80mg tablet
Plasma-concentration time data of salicylic acid
area under the plasma concentration-time curve from time zero to last measurable concentration time point for sublingual versus oral aspirin 80mg
Time frame: pre dose and up to 24 hour post dose
Peak plasma concentration of salicylic acid
Peak plasma concentration for sublingual versus oral aspirin 80mg
Time frame: pre dose and up to 24 hour post dose
Time to reach peak plasma concentration of salicylic acid
Tmax of sublingual versus oral aspirin 80mg
Time frame: pre dose and up to 24 hour post dose
Terminal phase elimination rate constant of salicylic acid
Terminal phase elimination rate constant of sublingual versus oral aspirin 80mg
Time frame: pre dose and up to 24 hour post dose
Terminal elimination half-life of salicylic acid
Terminal elimination half-life of sublingual versus oral aspirin 80mg
Time frame: pre dose and up to 24 hour post dose
Plasma concentration time data of thromboxane B2
Area under the curve for sublingual versus oral aspirin 80mg
Time frame: pre dose and up to 24 hour post dose
Platelet aggregation by impedance aggregometry
Differences in platelet aggregation with sublingual versus oral aspirin 80mg
Time frame: pre dose and up to 360 minutes post dose
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.