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Recruiting NCT07252284

NCT07252284 CHina Adrenal Venous saMPling InvestigatiON

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Clinical Trial Summary
NCT ID NCT07252284
Status Recruiting
Phase
Sponsor Chinese Academy of Medical Sciences, Fuwai Hospital
Condition Hyperaldosteronism
Study Type OBSERVATIONAL
Enrollment 5,000 participants
Start Date 2025-05-01
Primary Completion 2029-08-31

Trial Parameters

Condition Hyperaldosteronism
Sponsor Chinese Academy of Medical Sciences, Fuwai Hospital
Study Type OBSERVATIONAL
Phase N/A
Enrollment 5,000
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-05-01
Completion 2029-08-31
Interventions
adrenal venous sampling

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Brief Summary

Primary aldosteronism (PA) is a major cause of secondary hypertension, yet its optimal diagnosis and management remain challenging. This study comprehensively evaluates adrenal venous sampling (AVS), addressing key clinical, technical, and methodological issues, and aims to clarify the relationship between AVS-guided management and long-term clinical and biochemical outcomes to optimize patient care and prognosis.

Eligibility Criteria

Inclusion Criteria: 1. Patients with confirmed primary aldosteronism; 2. Patients undergoing adrenal venous sampling for subtype classification of primary aldosteronism. Exclusion Criteria: 1. Severe comorbidity, including stroke, myocardial infarction, heart failure, severe valvular heart disease, liver cirrhosis, and metastatic tumor within the previous 3 months; 2. An estimated glomerular filtration rate \<45 ml/min/1.73 m2, or serum creatinine \>176 μmol/L; 3. Patients who refuse adrenalectomy; 4. Suspected of having an adrenocortical carcinoma; 5. Allergy to contrast agent; 6. Pregnant, nursing, or planning to become pregnant

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