hypertension
Conditions
Interventions
None listed
Sponsors
Hamamatsu University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients treated with AML besylate tablets
Exclusion criteria
Exclusion criteria: Patients from whom written informed consent was not obtained
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of CYP3A activity by determining amlodipine and its two metabolites (dehydroamlodipine and O-des[2-aminoethyl]-O-carboxymethyl dehydroamlodipine) in Human Plasma | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of CYP3A activity by determining plasma 4beta-hydroxycholesterol as an endogenous CYP3A metric | — |
Countries
Japan
Contacts
Public ContactTakafumi Naito
Hamamatsu University School of Medicine Department of Hospital Pharmacy
Outcome results
None listed