Investigating the in vivo bioequivalence of Sildenafil 100 mg
Not Applicable
Recruiting
- Conditions
- In the present study, the products will be administered to healthy volunteers..
- Registration Number
- IRCT20210519051345N28
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 24
Inclusion Criteria
General Health (in terms of Liver, Heart and Kidney)
Exclusion Criteria
Smoking
History of cardiovascular disease, liver and kidney disease
Alcohol and drug addiction
History of drug allergy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Plasma concentration of drug. Timepoint: Before drug administration and 0.5-24 hours after drug administration in the following time intervals:0.5, 1,1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 24 h. Method of measurement: HPLC (High performance liquid chromatography).
- Secondary Outcome Measures
Name Time Method