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Research on the Precision Diagnosis and Treatment System for Primary Aldosteronism

Research on the Precision Diagnosis and Treatment System for Primary Aldosteronism

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101073
Enrollment
Unknown
Registered
2025-04-18
Start date
2025-03-16
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Hypertension

Interventions

Gold Standard:The laterality index (dominant aldosterone/cortisol ratio) in adrenal vein blood sampling is greater than 2, indicating unilateral dominant secretion.
Index test:1) The diagnostic value of peripheral blood 18 oxocortisol based on LC-MS/MS determination for unilateral dominant primary aldosteronism (PA)
2) The diagnostic value of standardized aldosterone ratios based on LC-MS/MS determination of steroids (17-a-hydroxyprogesterone, androstenedione, 18 oxycortisol, 18 hydroxycortisol, etc.) for unilate

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with primary aldosteronism; 2. Have the willingness to have adrenal gland surgery and the operation is feasible; 3. Sign the informed consent form for lateral adrenal vein blood collection; 4. Sign the written informed consent form for study enrollment.

Exclusion criteria

Exclusion criteria: 1) refusal to sign informed consent; 2) Patients diagnosed with other secondary hypertension (such as renal hypertension, renal artery stenosis, chromocytoma, Cushing's syndrome, etc., excluding sleep apnea syndrome); 3) eGFR <45 ml/min/1.73 m2, or patients with hepatic insufficiency (alanine aminotransferase and/or aspartate aminotransferase elevated more than 2.5 times the upper limit of normal); 4) Not stopping dihydropyridine calcium ion antagonists, B receptor blockers, angiotensin-converting enzyme inhibitors, angiotensin II receptor antagonists for at least 2 weeks, including aldosterone receptor antagonists (spironolactone, eplerenone), potassium-sparing diuretics (amiloride, triambenzine), potassium-excreting diuretics and licorice extract for at least 4 weeks; 5) Pregnant, trying to get pregnant, lactating women or patients who are currently taking sex hormones, glucocorticoids or are unable or unwilling to take safe contraceptive measures when undergoing examinations; 6) Patients at high risk of adrenal gland surgery who cannot tolerate surgery: 7) Patients without intention of adrenal surgery; 8) Conditions or medication regimens that are considered contraindications by the principal investigator.

Design outcomes

Primary

MeasureTime frame
18-oxocortisol;

Secondary

MeasureTime frame
Steroids (17-a-hydroxyprogesterone, androstenedione, 18 oxycortisol, 18 hydroxycortisol, etc.);

Countries

China

Contacts

Public ContactMa Wenjun

Fuwai Hospital, Chinese Academy of Medical Sciences

fuwaima@163.com+86 136 7118 8903

Outcome results

None listed

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