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Familial hypoaldosteronism

MONDO:0018541

Aldosterone synthase deficiency is a rare inherited defect of the final step of aldosterone biosynthesis (conversion of deoxycorticosterone to aldosterone).

9 clinical trials for this condition and its sub-types.

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Sub-types

Corticosterone methyloxidase type 1 deficiency (0) Corticosterone methyloxidase type 2 deficiency (0) Early-onset familial hypoaldosteronism (0) Familial hyperreninemic hypoaldosteronism type 2 (0) Late-onset familial hypoaldosteronism (0)

Broader categories

Disease (618) Endocrine system disorder (61) Human disease (14) Adrenal gland disorder (8) Hypoaldosteronism disease (1) Disease by body system or component (0)

Trials to join now! 6 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1

Tiny trial to see if a dye helps adrenal surgery

Knowledge-focused Not yet recruiting

This study will look at 12 people having surgery to remove an adrenal gland (adrenalectomy) using robotic or laparoscopic methods. Some surgeries will use a green dye called Indocyanine Green (ICG) to help the surgeon see better, while others will not. The main goal is to track c…

Sponsor: University of Roma La Sapienza • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:32 UTC