Skip to content

An open-label, single-arm clinical study to explore the efficacy, safety and efficacy of finerenone in patients with primary aldosteronism

An open-label, single-arm clinical study to explore the efficacy, safety and efficacy of finerenone in patients with primary aldosteronism

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090272
Enrollment
Unknown
Registered
2024-09-26
Start date
2023-12-30
Completion date
Unknown
Last updated
2024-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary aldosteronism

Interventions

Primary aldosteronism individuals:Use the drug of finerenone

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Clearly diagnosed with primary aldosteronism. 2.No administration of spironolactone, eplerenone, amiloride, or triamterene in the month prior to enrollment. 3.No use of antihypertensive medications other than calcium channel blockers and a-receptor blockers in the two weeks prior to enrollment.

Exclusion criteria

Exclusion criteria: Children/Minors; Adults with cognitive impairments or health conditions that render them incapable of providing informed consent; Patients in the terminal stage of illness; Prisoners or individuals subjected to forced labor; Pregnant or breastfeeding individuals; Blood potassium levels > 5.0 mmol/L; Coexisting Addison's disease; Individuals allergic to any component of norethisterone; Concurrent use of potent CYP3A4 inhibitors (itraconazole, ketoconazole, ritonavir, nelfinavir, cobicistat, clarithromycin, telithromycin, nefazodone) Estimated glomerular filtration rate (eGFR) < 25 ml/min/1.73m^2 Within 90 days of myocarditis, acute myocardial infarction, coronary artery revascularization, stroke, or transient ischemic attack

Design outcomes

Primary

MeasureTime frame
Serum potassium;

Secondary

MeasureTime frame
Blood pressure;24h Urine potassium;

Countries

China

Contacts

Public ContactMing Liu

Tianjin Medical University General Hospital

mingliu@tmu.edu.cn+86 183 2201 7516

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026