Hypertensive and/or Diabetic patients
Conditions
Interventions
None listed
Sponsors
Department of Metabolic Medicine, Graduate School of Medicine, Osaka University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1)Hypertensive and/or diabetic patients who understand the study procedures using explanatory notes and have given written informed consent to participate in the study, and, 2)Patients have not yet received candesartan and pioglitazone.
Exclusion criteria
Exclusion criteria: 1)Contraindications of candesartan 2)Contraindications of Pioglitazone
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes of TBARS(Thiobarbituric acid reactive substances), highsensitive CRP, and Adiponectin at the completion of treatment form baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes of waist circumference, glucose-lipid metabolic parameters, and blood pressure | — |
Countries
Japan
Contacts
Public ContactKen Kishida
Osaka University Metabolic medicine
Outcome results
None listed