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A clinical study of the safety and efficacy of a novel diagnostic test for primary aldosteronism

A clinical study of the safety and efficacy of a novel diagnostic test for primary aldosteronism

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045868
Enrollment
Unknown
Registered
2021-04-25
Start date
2021-05-17
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

Primary aldosteronism

Interventions

Gold Standard:Normal saline test, captopril inhibition test, adrenal blood collection
Index test:Inhibition&#32
test&#32
of&#32
dexamethasone&#32
valsartan

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with persistent hypertension (>150/100mmHg, 1mmHg=0.133kPs); Patients whose blood pressure (>140/90mmHg) cannot be controlled with 3 conventional antihypertensive drugs (including diuretics); Patients with blood pressure (= 4 antihypertensive drugs and newly diagnosed hypertension patients. 2. Patients with hypertension complicated with spontaneous or diuretic hypokalemia. 3. Patients with hypertension complicated with adrenal accidental tumor. 4. Family history of early onset hypertension or early onset (<40 years old) hypertensive patients with a family history of cerebrovascular accident. 5. First-degree relatives with hypertension in patients with PHA. 6. Patients with hypertension complicated with obstructive sleep apnea.

Exclusion criteria

Exclusion criteria: 1. Complicated pregnant and lactating women, taking estrogen or oral contraceptives; 2. Complicated with severe heart (grade III or above), lung, liver, kidney (eGFR<30ml/min/1.73m2) and other diseases; 3. Patients with secondary hypertension whose etiology has been identified, such as: Cushing syndrome, subclinical Cushing syndrome, pheochromocytoma, renal artery stenosis, etc; 4. Patients who cannot tolerate ACEI; 5. Patients with clear use of non-antihypertensive drugs affecting RAAS results: such as licorice, etc.

Design outcomes

Primary

MeasureTime frame
Plasma aldosterone concentration;Plasma renin concentration;Adrenocorticotropic hormone;Blood cortisol;

Countries

China

Contacts

Public ContactChen Tao

West China Hospital of Sichuan University

drchentao@qq.com+86 18980606758

Outcome results

None listed

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