Finerenone for Patients With Primary Aldosteronism (FAIRY)

Status Recruiting

Clinical Trial Summary

Using spironolactone as the control, to assess the efficacy and safety of finerenone in patients with primary aldosteronism(PA).

Clinical Trial Description

This is a multicenter, randomized study designed to evaluate efficacy and safety of finerenone in patients with PA. PA patients are randomly divided into two groups and treated with finerenone or spironolactone for 12 weeks. Spironolactone will be used as the control, while outcome will be assessed after 12-week treatment. Both drugs will be started at 20mg per day, Dose will be adjusted every four weeks to achieve the targeted blood pressure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06457074
Study type	Interventional
Source	Chongqing Medical University
Contact	Shumin Yang
Phone	02389011552
Email	443068494@qq.com
Status	Recruiting
Phase	Phase 4
Start date	June 4, 2024
Completion date	June 1, 2026

View Details

See also
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