Primary aldsteronism,or Cushing disease
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with an endocrinological diagnosis of primary aldosteronism or Cushing's disease who will undergo AVS or IPS/CS sampling for the purpose of localization. 2. Patients aged 18 years or older. 3. Patients who have received a thorough explanation of participation in this study and have provided their voluntary written consent with a full understanding.
Exclusion criteria
Exclusion criteria: 1. Pregnant or lactating patients 2. Patients in whom it is difficult to collect an additional 5 ml of blood from each of the left and right (or central/peripheral) venous sampling sites 3. Patients who are otherwise deemed inappropriate for this study by the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increace in rate of tumor localization by adding genetic analyses using cell-free DNA obtained from tumor venous sampling in patients with primary aldsteronism or Cushing disease. | — |
Countries
Japan
Contacts
Nagasaki University Hospital Endocrinology and Metabolism