endocrine and metabolic disorder
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient who is diagnosed endocrinological disease Patients whose content is obtained in written form
Exclusion criteria
Exclusion criteria: Younger than 20 years old Pregnant or lactating women Patient in endocrinological emergency Severe mental problems not suitable for the study Inability to participate in the study as assessed by the investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes from baseline in organ specific insulin sensitivity and glucagon response during a euglycemic hyperinsulinemic clamp study | — |
Secondary
| Measure | Time frame |
|---|---|
| 1Change from baseline in fasting plasma glucose level and glucose metabolism assessed with arginine tolerance test 2Change from baseline in body composition 3Change from baseline in vital sign 4Change from baseline in hormone levels of endocrine and metabolic disorder 5Change from baseline in medication 6Change from baseline in liver function 7Changes from baseline in lipid profile 8Changes from baseline in renal function and electrolyte balance 9Changes from baseline in hepatokine levels 10Changes from baseline in oxidative and non-oxidative glucose disposal, respiratory quotients, and energy expenditure | — |
Countries
Japan
Contacts
Kanazawa university hospital Department of Endocrinology and metabolism