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Xiangya Primary Aldosteronism Precision Cohort

Xiangya Primary Aldosteronism Precision Cohort

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115724
Enrollment
Unknown
Registered
2025-12-30
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Primsry aldosteronism

Interventions

Observation group:N/A

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged over 18 years, regardless of gender; 2.Voluntarily agree to participate in this study and sign an informed consent form; 3.Positive PA screening, defined as an upright plasma aldosterone-to-renin ratio (ARR) >=20 (pg/ml)/(µIU/ml) or ARR >=30 (ng/dL)/(ng/ml/hr), with at least one confirmatory test being positive (plasma aldosterone >=110 pg/ml after captopril suppression test (CCT) or plasma aldosterone >=100 pg/ml after seated saline infusion test (SIT)). 4.Subtype diagnosis: UPA (meets any of the following criteria): AVS indicates unilateral lesion; Positive visual imaging on 68Ga-Pentixafor PET/CT, with SUVmax>=7.65 or LCR >=1.60 or LLR >=3.36; Postoperative pathology consistent with UPA HISTALDO classification. BPA (meets any of the following criteria): AVS indicates bilateral lesions; Negative or mildly increased uptake on 68Ga-Pentixafor PET/CT, with SUVmax <7.65, LCR <1.60, and LLR <3.36.

Exclusion criteria

Exclusion criteria: 1.Refusal to participate in the trial, or inability of the patient or close relatives to understand or sign the informed consent form. 2.Coexistence of other common types of secondary hypertension, such as renal artery stenosis, renal parenchymal hypertension, pheochromocytoma, hypercortisolism, etc. 3.Coexistence of malignant tumors or severe cardiac, pulmonary, renal, or hepatic dysfunction. 4.Women who are pregnant or breastfeeding, those planning to become pregnant during the trial period, and women at high risk of pregnancy without taking any contraceptive measures.

Design outcomes

Primary

MeasureTime frame
Accuracy of the prediction model for PA subtype diagnosis;Accuracy of the prognostic model;Proportion of clinical complete remission;

Secondary

MeasureTime frame
Percentage of biochemical complete remission;

Countries

China

Contacts

Public ContactLuo Xianghang / Jiang Tiejian

Xiangya Hospital, Central South University

xianghangluo@csu.edu.cn+86 731 8975 3727

Outcome results

None listed

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