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Efficacy and Safety of Finerenone in Patients With Primary Aldosteronism

Primary Aldosteronism Clinical Trial

Official title:
Efficacy and Safety of Finerenone in Patients With Primary Aldosteronism: a Randomized, Controlled Trial

Clinical Trial Summary

To study the efficacy and safety of finerenone in patients with primary aldosteronism

Clinical Trial Description

This is a prospective and randomized study involving patients with primary aldosteronism(PA). All paticipants will be randomized into finerenone group(Intervention group) and spironolactone group(Control group) and to compare the antihypertensive effect in patients with PA. If the self-measured blood pressure of patients at home continues to be greater than 140/90 mmHg at 2-4 weeks, spironolactone or finerenone should be increased to 40mg qd, and electrolytes should be reviewed at 2 weeks after dosed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05924620
Study type Interventional
Source Chongqing Medical University
Contact
Status Completed
Phase Phase 4
Start date June 21, 2023
Completion date March 12, 2024
View Details
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